Name: rs34544244
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs34544244

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:112280344-112280367 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₇ / dup(T)₂₂ / dup(T)₂₃ / ins(T)₃₄ / ins(T)₃₅ / ins(T)₄₀
Variation Type: Indel Insertion and Deletion
Frequency: (T)₂₄=0.4119 (2063/5008, 1000G)
del(T)₄=0.1645 (768/4668, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TIFA : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	4668	TTTTTTTTTTTTTTTTTTTTTTTT=0.6527	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1645, TTTTTTTTTTTTTTTTTTTTTTT=0.1510, TTTTTTTTTTTTTTTTTTTTT=0.0261, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0039, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.704854	0.026537	0.268608	0
European	Sub	4592	TTTTTTTTTTTTTTTTTTTTTTTT=0.6479	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1670, TTTTTTTTTTTTTTTTTTTTTTT=0.1529, TTTTTTTTTTTTTTTTTTTTT=0.0266, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0039, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.698013	0.027152	0.274834	0
African	Sub	24	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTT=0.78	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.06, TTTTTTTTTTTTTTTTTTTTTTT=0.17, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(T)₂₄=0.4119	del(T)₄=0.5881
1000Genomes	African	Sub	1322	(T)₂₄=0.2231	del(T)₄=0.7769
1000Genomes	East Asian	Sub	1008	(T)₂₄=0.4127	del(T)₄=0.5873
1000Genomes	Europe	Sub	1006	(T)₂₄=0.5199	del(T)₄=0.4801
1000Genomes	South Asian	Sub	978	(T)₂₄=0.528	del(T)₄=0.472
1000Genomes	American	Sub	694	(T)₂₄=0.451	del(T)₄=0.549
Allele Frequency Aggregator	Total	Global	4668	(T)₂₄=0.6527	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.1645, delTTT=0.0261, delTT=0.0000, delT=0.1510, dupT=0.0000, dupTT=0.0000, dup(T)₂₃=0.0039, ins(T)₃₅=0.0017
Allele Frequency Aggregator	European	Sub	4592	(T)₂₄=0.6479	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.1670, delTTT=0.0266, delTT=0.0000, delT=0.1529, dupT=0.0000, dupTT=0.0000, dup(T)₂₃=0.0039, ins(T)₃₅=0.0017
Allele Frequency Aggregator	African	Sub	24	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₂₃=0.00, ins(T)₃₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	22	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₂₃=0.00, ins(T)₃₅=0.00
Allele Frequency Aggregator	Other	Sub	18	(T)₂₄=0.78	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.06, delTTT=0.00, delTT=0.00, delT=0.17, dupT=0.00, dupTT=0.00, dup(T)₂₃=0.00, ins(T)₃₅=0.00
Allele Frequency Aggregator	Asian	Sub	8	(T)₂₄=1.0	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dup(T)₂₃=0.0, ins(T)₃₅=0.0
Allele Frequency Aggregator	Latin American 1	Sub	4	(T)₂₄=1.0	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dup(T)₂₃=0.0, ins(T)₃₅=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₄=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₁₀=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dup(T)₂₃=0, ins(T)₃₅=0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 4	NC_000004.12:g.112280355_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280356_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280357_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280358_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280360_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280361_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280362_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280363_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280364_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280365_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280366_112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280367del
GRCh38.p14 chr 4	NC_000004.12:g.112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280366_112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280365_112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280364_112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280363_112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280361_112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280346_112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280345_112280367dup
GRCh38.p14 chr 4	NC_000004.12:g.112280367_112280368insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.112280367_112280368insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.112280367_112280368insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.113201511_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201512_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201513_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201514_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201516_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201517_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201518_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201519_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201520_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201521_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201522_113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201523del
GRCh37.p13 chr 4	NC_000004.11:g.113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201522_113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201521_113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201520_113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201519_113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201517_113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201502_113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201501_113201523dup
GRCh37.p13 chr 4	NC_000004.11:g.113201523_113201524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.113201523_113201524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.113201523_113201524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: TIFA, TRAF interacting protein with forkhead associated domain (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TIFA transcript	NM_052864.3:c.-18-1922_-1… NM_052864.3:c.-18-1922_-18-1910del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₄=	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₇	dup(T)₂₂	dup(T)₂₃	ins(T)₃₄	ins(T)₃₅	ins(T)₄₀
GRCh38.p14 chr 4	NC_000004.12:g.112280344_112280367=	NC_000004.12:g.112280355_112280367del	NC_000004.12:g.112280356_112280367del	NC_000004.12:g.112280357_112280367del	NC_000004.12:g.112280358_112280367del	NC_000004.12:g.112280360_112280367del	NC_000004.12:g.112280361_112280367del	NC_000004.12:g.112280362_112280367del	NC_000004.12:g.112280363_112280367del	NC_000004.12:g.112280364_112280367del	NC_000004.12:g.112280365_112280367del	NC_000004.12:g.112280366_112280367del	NC_000004.12:g.112280367del	NC_000004.12:g.112280367dup	NC_000004.12:g.112280366_112280367dup	NC_000004.12:g.112280365_112280367dup	NC_000004.12:g.112280364_112280367dup	NC_000004.12:g.112280363_112280367dup	NC_000004.12:g.112280361_112280367dup	NC_000004.12:g.112280346_112280367dup	NC_000004.12:g.112280345_112280367dup	NC_000004.12:g.112280367_112280368insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.112280367_112280368insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.112280367_112280368insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.113201500_113201523=	NC_000004.11:g.113201511_113201523del	NC_000004.11:g.113201512_113201523del	NC_000004.11:g.113201513_113201523del	NC_000004.11:g.113201514_113201523del	NC_000004.11:g.113201516_113201523del	NC_000004.11:g.113201517_113201523del	NC_000004.11:g.113201518_113201523del	NC_000004.11:g.113201519_113201523del	NC_000004.11:g.113201520_113201523del	NC_000004.11:g.113201521_113201523del	NC_000004.11:g.113201522_113201523del	NC_000004.11:g.113201523del	NC_000004.11:g.113201523dup	NC_000004.11:g.113201522_113201523dup	NC_000004.11:g.113201521_113201523dup	NC_000004.11:g.113201520_113201523dup	NC_000004.11:g.113201519_113201523dup	NC_000004.11:g.113201517_113201523dup	NC_000004.11:g.113201502_113201523dup	NC_000004.11:g.113201501_113201523dup	NC_000004.11:g.113201523_113201524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.113201523_113201524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.113201523_113201524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TIFA transcript	NM_052864.2:c.-18-1910=	NM_052864.2:c.-18-1922_-18-1910del	NM_052864.2:c.-18-1921_-18-1910del	NM_052864.2:c.-18-1920_-18-1910del	NM_052864.2:c.-18-1919_-18-1910del	NM_052864.2:c.-18-1917_-18-1910del	NM_052864.2:c.-18-1916_-18-1910del	NM_052864.2:c.-18-1915_-18-1910del	NM_052864.2:c.-18-1914_-18-1910del	NM_052864.2:c.-18-1913_-18-1910del	NM_052864.2:c.-18-1912_-18-1910del	NM_052864.2:c.-18-1911_-18-1910del	NM_052864.2:c.-18-1910del	NM_052864.2:c.-18-1910dup	NM_052864.2:c.-18-1911_-18-1910dup	NM_052864.2:c.-18-1912_-18-1910dup	NM_052864.2:c.-18-1913_-18-1910dup	NM_052864.2:c.-18-1914_-18-1910dup	NM_052864.2:c.-18-1916_-18-1910dup	NM_052864.2:c.-18-1931_-18-1910dup	NM_052864.2:c.-18-1932_-18-1910dup	NM_052864.2:c.-18-1910_-18-1909insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_052864.2:c.-18-1910_-18-1909insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_052864.2:c.-18-1910_-18-1909insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TIFA transcript	NM_052864.3:c.-18-1910=	NM_052864.3:c.-18-1922_-18-1910del	NM_052864.3:c.-18-1921_-18-1910del	NM_052864.3:c.-18-1920_-18-1910del	NM_052864.3:c.-18-1919_-18-1910del	NM_052864.3:c.-18-1917_-18-1910del	NM_052864.3:c.-18-1916_-18-1910del	NM_052864.3:c.-18-1915_-18-1910del	NM_052864.3:c.-18-1914_-18-1910del	NM_052864.3:c.-18-1913_-18-1910del	NM_052864.3:c.-18-1912_-18-1910del	NM_052864.3:c.-18-1911_-18-1910del	NM_052864.3:c.-18-1910del	NM_052864.3:c.-18-1910dup	NM_052864.3:c.-18-1911_-18-1910dup	NM_052864.3:c.-18-1912_-18-1910dup	NM_052864.3:c.-18-1913_-18-1910dup	NM_052864.3:c.-18-1914_-18-1910dup	NM_052864.3:c.-18-1916_-18-1910dup	NM_052864.3:c.-18-1931_-18-1910dup	NM_052864.3:c.-18-1932_-18-1910dup	NM_052864.3:c.-18-1910_-18-1909insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_052864.3:c.-18-1910_-18-1909insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_052864.3:c.-18-1910_-18-1909insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

48 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95365800	Dec 05, 2013 (144)
2	PJP	ss295182820	May 09, 2011 (137)
3	PJP	ss295182821	May 09, 2011 (137)
4	1000GENOMES	ss1372641316	Aug 21, 2014 (142)
5	SWEGEN	ss2995354347	Nov 08, 2017 (151)
6	EVA_DECODE	ss3712828131	Jul 13, 2019 (153)
7	EVA_DECODE	ss3712828132	Jul 13, 2019 (153)
8	EVA_DECODE	ss3712828133	Jul 13, 2019 (153)
9	EVA_DECODE	ss3712828134	Jul 13, 2019 (153)
10	EVA_DECODE	ss3712828135	Jul 13, 2019 (153)
11	PACBIO	ss3784825159	Jul 13, 2019 (153)
12	PACBIO	ss3790266117	Jul 13, 2019 (153)
13	PACBIO	ss3790266118	Jul 13, 2019 (153)
14	PACBIO	ss3795141495	Jul 13, 2019 (153)
15	PACBIO	ss3795141496	Jul 13, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3805417400	Jul 13, 2019 (153)
17	GNOMAD	ss4118297048	Apr 26, 2021 (155)
18	GNOMAD	ss4118297049	Apr 26, 2021 (155)
19	GNOMAD	ss4118297050	Apr 26, 2021 (155)
20	GNOMAD	ss4118297051	Apr 26, 2021 (155)
21	GNOMAD	ss4118297052	Apr 26, 2021 (155)
22	GNOMAD	ss4118297053	Apr 26, 2021 (155)
23	GNOMAD	ss4118297054	Apr 26, 2021 (155)
24	GNOMAD	ss4118297055	Apr 26, 2021 (155)
25	GNOMAD	ss4118297056	Apr 26, 2021 (155)
26	GNOMAD	ss4118297057	Apr 26, 2021 (155)
27	GNOMAD	ss4118297058	Apr 26, 2021 (155)
28	GNOMAD	ss4118297059	Apr 26, 2021 (155)
29	GNOMAD	ss4118297060	Apr 26, 2021 (155)
30	GNOMAD	ss4118297061	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5167465713	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5167465714	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5167465715	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5167465716	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5167465717	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5167465718	Apr 26, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5260594744	Oct 13, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5260594745	Oct 13, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5260594746	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5260594747	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5260594748	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5260594749	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5702307495	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5702307496	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5702307497	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5702307498	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5702307499	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5702307500	Oct 13, 2022 (156)
49	1000Genomes	NC_000004.11 - 113201500	Oct 12, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 161439614 (NC_000004.12:112280343::TT 132/70246) Row 161439615 (NC_000004.12:112280343::TTT 17/70250) Row 161439616 (NC_000004.12:112280343::TTTT 2/70244)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 25435020 (NC_000004.11:113201499:TTTT: 5613/16618) Row 25435021 (NC_000004.11:113201499:T: 1573/16618) Row 25435022 (NC_000004.11:113201499:TTTTT: 62/16618)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 25435020 (NC_000004.11:113201499:TTTT: 5613/16618) Row 25435021 (NC_000004.11:113201499:T: 1573/16618) Row 25435022 (NC_000004.11:113201499:TTTTT: 62/16618)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 25435020 (NC_000004.11:113201499:TTTT: 5613/16618) Row 25435021 (NC_000004.11:113201499:T: 1573/16618) Row 25435022 (NC_000004.11:113201499:TTTTT: 62/16618)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 25435020 (NC_000004.11:113201499:TTTT: 5613/16618) Row 25435021 (NC_000004.11:113201499:T: 1573/16618) Row 25435022 (NC_000004.11:113201499:TTTTT: 62/16618)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 25435020 (NC_000004.11:113201499:TTTT: 5613/16618) Row 25435021 (NC_000004.11:113201499:T: 1573/16618) Row 25435022 (NC_000004.11:113201499:TTTTT: 62/16618)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 25435020 (NC_000004.11:113201499:TTTT: 5613/16618) Row 25435021 (NC_000004.11:113201499:T: 1573/16618) Row 25435022 (NC_000004.11:113201499:TTTTT: 62/16618)...	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 36144599 (NC_000004.12:112280343:TTTT: 12479/28234) Row 36144600 (NC_000004.12:112280343:T: 3753/28234) Row 36144601 (NC_000004.12:112280343:TTTTT: 131/28234)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 36144599 (NC_000004.12:112280343:TTTT: 12479/28234) Row 36144600 (NC_000004.12:112280343:T: 3753/28234) Row 36144601 (NC_000004.12:112280343:TTTTT: 131/28234)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 36144599 (NC_000004.12:112280343:TTTT: 12479/28234) Row 36144600 (NC_000004.12:112280343:T: 3753/28234) Row 36144601 (NC_000004.12:112280343:TTTTT: 131/28234)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 36144599 (NC_000004.12:112280343:TTTT: 12479/28234) Row 36144600 (NC_000004.12:112280343:T: 3753/28234) Row 36144601 (NC_000004.12:112280343:TTTTT: 131/28234)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 36144599 (NC_000004.12:112280343:TTTT: 12479/28234) Row 36144600 (NC_000004.12:112280343:T: 3753/28234) Row 36144601 (NC_000004.12:112280343:TTTTT: 131/28234)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 36144599 (NC_000004.12:112280343:TTTT: 12479/28234) Row 36144600 (NC_000004.12:112280343:T: 3753/28234) Row 36144601 (NC_000004.12:112280343:TTTTT: 131/28234)...	-	Oct 13, 2022 (156)
76	ALFA	NC_000004.12 - 112280344	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs70958455	Jul 30, 2012 (137)
rs72182878	May 11, 2012 (137)
rs138743746	May 04, 2012 (137)
rs397995005	Jul 01, 2015 (144)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4118297061	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4118297060	NC_000004.12:112280343:TTTTTTTTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4118297059	NC_000004.12:112280343:TTTTTTTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4118297058	NC_000004.12:112280343:TTTTTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4118297057	NC_000004.12:112280343:TTTTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5167465715	NC_000004.11:113201499:TTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3712828131, ss5260594748, ss5702307497	NC_000004.12:112280343:TTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
22785868, ss1372641316, ss2995354347, ss3784825159, ss3790266117, ss3795141495, ss5167465713	NC_000004.11:113201499:TTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3805417400, ss5260594745, ss5702307495	NC_000004.12:112280343:TTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3712828132	NC_000004.12:112280344:TTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3790266118, ss3795141496, ss5167465716	NC_000004.11:113201499:TTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5260594746, ss5702307499	NC_000004.12:112280343:TTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3712828133	NC_000004.12:112280345:TTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5167465718	NC_000004.11:113201499:TT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5260594749, ss5702307500	NC_000004.12:112280343:TT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3712828134	NC_000004.12:112280346:TT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss295182820	NC_000004.10:113420948:T:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295182821	NC_000004.10:113420971:T:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5167465714	NC_000004.11:113201499:T:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5260594744, ss5702307496	NC_000004.12:112280343:T:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3712828135	NC_000004.12:112280347:T:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95365800	NT_016354.19:37749243:T:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5167465717	NC_000004.11:113201499::T	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5260594747, ss5702307498	NC_000004.12:112280343::T	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297048	NC_000004.12:112280343::TT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297049	NC_000004.12:112280343::TTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297050	NC_000004.12:112280343::TTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297051	NC_000004.12:112280343::TTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297052	NC_000004.12:112280343::TTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297053	NC_000004.12:112280343::TTTTTTTTTT… NC_000004.12:112280343::TTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297054	NC_000004.12:112280343::TTTTTTTTTT… NC_000004.12:112280343::TTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297055	NC_000004.12:112280343::TTTTTTTTTT… NC_000004.12:112280343::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
897916926	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4118297056	NC_000004.12:112280343::TTTTTTTTTT… NC_000004.12:112280343::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3439583398	NC_000004.12:112280343:TTTTTT:	NC_000004.12:112280343:TTTTTTTTTTT… NC_000004.12:112280343:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs34544244

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34544244