Name: rs1351505374
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.

rs1351505374

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:53073456 (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: T>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.000011 (3/264690, TOPMED)
A=0.000009 (2/228928, GnomAD_exome)
A=0.00000 (0/14050, ALFA) (+ 2 more)
C=0.00000 (0/14050, ALFA)
G=0.0044 (8/1832, Korea1K)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF160 : Stop Gained
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	HWEP
Total	Global	14050	T=1.00000	A=0.00000, C=0.00000	1.0	N/A
European	Sub	9690	T=1.0000	A=0.0000, C=0.0000	1.0	N/A
African	Sub	2898	T=1.0000	A=0.0000, C=0.0000	1.0	N/A
African Others	Sub	114	T=1.000	A=0.000, C=0.000	1.0	N/A
African American	Sub	2784	T=1.0000	A=0.0000, C=0.0000	1.0	N/A
Asian	Sub	112	T=1.000	A=0.000, C=0.000	1.0	N/A
East Asian	Sub	86	T=1.00	A=0.00, C=0.00	1.0	N/A
Other Asian	Sub	26	T=1.00	A=0.00, C=0.00	1.0	N/A
Latin American 1	Sub	146	T=1.000	A=0.000, C=0.000	1.0	N/A
Latin American 2	Sub	610	T=1.000	A=0.000, C=0.000	1.0	N/A
South Asian	Sub	98	T=1.00	A=0.00, C=0.00	1.0	N/A
Other	Sub	496	T=1.000	A=0.000, C=0.000	1.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.999989	A=0.000011
gnomAD - Exomes	Global	Study-wide	228928	T=0.999991	A=0.000009
gnomAD - Exomes	European	Sub	117234	T=0.999983	A=0.000017
gnomAD - Exomes	Asian	Sub	47866	T=1.00000	A=0.00000
gnomAD - Exomes	American	Sub	34270	T=1.00000	A=0.00000
gnomAD - Exomes	African	Sub	13886	T=1.00000	A=0.00000
gnomAD - Exomes	Ashkenazi Jewish	Sub	9822	T=1.0000	A=0.0000
gnomAD - Exomes	Other	Sub	5850	T=1.0000	A=0.0000
Allele Frequency Aggregator	Total	Global	14050	T=1.00000	A=0.00000, C=0.00000
Allele Frequency Aggregator	European	Sub	9690	T=1.0000	A=0.0000, C=0.0000
Allele Frequency Aggregator	African	Sub	2898	T=1.0000	A=0.0000, C=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	T=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	Other	Sub	496	T=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	T=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	Asian	Sub	112	T=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	South Asian	Sub	98	T=1.00	A=0.00, C=0.00
Korean Genome Project	KOREAN	Study-wide	1832	T=0.9956	G=0.0044

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 19	NC_000019.10:g.53073456T>A
GRCh38.p14 chr 19	NC_000019.10:g.53073456T>C
GRCh38.p14 chr 19	NC_000019.10:g.53073456T>G
GRCh37.p13 chr 19	NC_000019.9:g.53576709T>A
GRCh37.p13 chr 19	NC_000019.9:g.53576709T>C
GRCh37.p13 chr 19	NC_000019.9:g.53576709T>G

Gene: ZNF160, zinc finger protein 160 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF160 transcript variant 3	NM_001102603.2:c.271+684A… NM_001102603.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 4	NM_001322128.2:c.271+684A… NM_001322128.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 5	NM_001322129.2:c.271+684A… NM_001322129.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 6	NM_001322130.2:c.271+684A… NM_001322130.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 7	NM_001322131.2:c.271+684A… NM_001322131.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 8	NM_001322132.2:c.271+684A… NM_001322132.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 9	NM_001322133.2:c.271+684A… NM_001322133.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 10	NM_001322134.2:c.271+684A… NM_001322134.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 11	NM_001322135.2:c.271+684A… NM_001322135.2:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 12	NM_001322136.1:c.271+684A… NM_001322136.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 13	NM_001322137.2:c.163+684A… NM_001322137.2:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant 14	NM_001322138.2:c.163+684A… NM_001322138.2:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant 15	NM_001322139.2:c.163+684A… NM_001322139.2:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant 1	NM_033288.4:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 2	NM_198893.3:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant 16	NM_001322125.2:c.325A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform c	NP_001309054.1:p.Lys109Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant 16	NM_001322125.2:c.325A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform c	NP_001309054.1:p.Lys109Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant 16	NM_001322125.2:c.325A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform c	NP_001309054.1:p.Lys109Gln	K (Lys) > Q (Gln)	Missense Variant
ZNF160 transcript variant 17	NM_001322126.2:c.325A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform c	NP_001309055.1:p.Lys109Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant 17	NM_001322126.2:c.325A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform c	NP_001309055.1:p.Lys109Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant 17	NM_001322126.2:c.325A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform c	NP_001309055.1:p.Lys109Gln	K (Lys) > Q (Gln)	Missense Variant
ZNF160 transcript variant X1	XM_047439616.1:c.271+684A… XM_047439616.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant X2	XM_047439617.1:c.328+684A… XM_047439617.1:c.328+684A>T	N/A	Intron Variant
ZNF160 transcript variant X3	XM_047439618.1:c.271+684A… XM_047439618.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant X4	XM_047439619.1:c.271+684A… XM_047439619.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant X5	XM_047439620.1:c.271+684A… XM_047439620.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant X6	XM_047439621.1:c.271+684A… XM_047439621.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant X7	XM_047439622.1:c.271+684A… XM_047439622.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant X8	XM_047439623.1:c.271+684A… XM_047439623.1:c.271+684A>T	N/A	Intron Variant
ZNF160 transcript variant X9	XM_047439624.1:c.328+684A… XM_047439624.1:c.328+684A>T	N/A	Intron Variant
ZNF160 transcript variant X10	XM_047439625.1:c.163+684A… XM_047439625.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X11	XM_047439626.1:c.163+684A… XM_047439626.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X12	XM_047439627.1:c.163+684A… XM_047439627.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X13	XM_047439628.1:c.163+684A… XM_047439628.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X14	XM_047439629.1:c.163+684A… XM_047439629.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X15	XM_047439630.1:c.163+684A… XM_047439630.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X16	XM_047439631.1:c.163+684A… XM_047439631.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X17	XM_047439632.1:c.163+684A… XM_047439632.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X18	XM_047439633.1:c.163+684A… XM_047439633.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X19	XM_047439634.1:c.163+684A… XM_047439634.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X20	XM_047439635.1:c.163+684A… XM_047439635.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X21	XM_047439636.1:c.163+684A… XM_047439636.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X22	XM_047439637.1:c.163+684A… XM_047439637.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X23	XM_047439638.1:c.163+684A… XM_047439638.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X24	XM_047439639.1:c.163+684A… XM_047439639.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X25	XM_047439640.1:c.163+684A… XM_047439640.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X26	XM_047439641.1:c.163+684A… XM_047439641.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X27	XM_047439642.1:c.163+684A… XM_047439642.1:c.163+684A>T	N/A	Intron Variant
ZNF160 transcript variant X28	XM_017027447.3:c.382A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform X4	XP_016882936.1:p.Lys128Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant X28	XM_017027447.3:c.382A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform X4	XP_016882936.1:p.Lys128Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant X28	XM_017027447.3:c.382A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform X4	XP_016882936.1:p.Lys128Gln	K (Lys) > Q (Gln)	Missense Variant
ZNF160 transcript variant X29	XM_047439643.1:c.325A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295599.1:p.Lys109Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant X29	XM_047439643.1:c.325A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295599.1:p.Lys109Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant X29	XM_047439643.1:c.325A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295599.1:p.Lys109Gln	K (Lys) > Q (Gln)	Missense Variant
ZNF160 transcript variant X30	XM_047439644.1:c.325A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295600.1:p.Lys109Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant X30	XM_047439644.1:c.325A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295600.1:p.Lys109Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant X30	XM_047439644.1:c.325A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295600.1:p.Lys109Gln	K (Lys) > Q (Gln)	Missense Variant
ZNF160 transcript variant X31	XM_047439645.1:c.325A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295601.1:p.Lys109Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant X31	XM_047439645.1:c.325A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295601.1:p.Lys109Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant X31	XM_047439645.1:c.325A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295601.1:p.Lys109Gln	K (Lys) > Q (Gln)	Missense Variant
ZNF160 transcript variant X32	XM_047439646.1:c.325A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295602.1:p.Lys109Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant X32	XM_047439646.1:c.325A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295602.1:p.Lys109Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant X32	XM_047439646.1:c.325A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_047295602.1:p.Lys109Gln	K (Lys) > Q (Gln)	Missense Variant
ZNF160 transcript variant X33	XM_017027448.3:c.325A>T	K [AAA] > * [TAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_016882937.1:p.Lys109Ter	K (Lys) > * (Ter)	Stop Gained
ZNF160 transcript variant X33	XM_017027448.3:c.325A>G	K [AAA] > E [GAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_016882937.1:p.Lys109Glu	K (Lys) > E (Glu)	Missense Variant
ZNF160 transcript variant X33	XM_017027448.3:c.325A>C	K [AAA] > Q [CAA]	Coding Sequence Variant
zinc finger protein 160 isoform X5	XP_016882937.1:p.Lys109Gln	K (Lys) > Q (Gln)	Missense 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=	A	C	G
GRCh38.p14 chr 19	NC_000019.10:g.53073456=	NC_000019.10:g.53073456T>A	NC_000019.10:g.53073456T>C	NC_000019.10:g.53073456T>G
GRCh37.p13 chr 19	NC_000019.9:g.53576709=	NC_000019.9:g.53576709T>A	NC_000019.9:g.53576709T>C	NC_000019.9:g.53576709T>G
ZNF160 transcript variant X33	XM_017027448.3:c.325=	XM_017027448.3:c.325A>T	XM_017027448.3:c.325A>G	XM_017027448.3:c.325A>C
ZNF160 transcript variant X2	XM_017027448.2:c.325=	XM_017027448.2:c.325A>T	XM_017027448.2:c.325A>G	XM_017027448.2:c.325A>C
ZNF160 transcript variant X4	XM_017027448.1:c.325=	XM_017027448.1:c.325A>T	XM_017027448.1:c.325A>G	XM_017027448.1:c.325A>C
ZNF160 transcript variant X28	XM_017027447.3:c.382=	XM_017027447.3:c.382A>T	XM_017027447.3:c.382A>G	XM_017027447.3:c.382A>C
ZNF160 transcript variant X1	XM_017027447.2:c.382=	XM_017027447.2:c.382A>T	XM_017027447.2:c.382A>G	XM_017027447.2:c.382A>C
ZNF160 transcript variant X3	XM_017027447.1:c.382=	XM_017027447.1:c.382A>T	XM_017027447.1:c.382A>G	XM_017027447.1:c.382A>C
ZNF160 transcript variant 17	NM_001322126.2:c.325=	NM_001322126.2:c.325A>T	NM_001322126.2:c.325A>G	NM_001322126.2:c.325A>C
ZNF160 transcript variant 17	NM_001322126.1:c.325=	NM_001322126.1:c.325A>T	NM_001322126.1:c.325A>G	NM_001322126.1:c.325A>C
ZNF160 transcript variant 16	NM_001322125.2:c.325=	NM_001322125.2:c.325A>T	NM_001322125.2:c.325A>G	NM_001322125.2:c.325A>C
ZNF160 transcript variant 16	NM_001322125.1:c.325=	NM_001322125.1:c.325A>T	NM_001322125.1:c.325A>G	NM_001322125.1:c.325A>C
ZNF160 transcript variant X29	XM_047439643.1:c.325=	XM_047439643.1:c.325A>T	XM_047439643.1:c.325A>G	XM_047439643.1:c.325A>C
ZNF160 transcript variant X32	XM_047439646.1:c.325=	XM_047439646.1:c.325A>T	XM_047439646.1:c.325A>G	XM_047439646.1:c.325A>C
ZNF160 transcript variant X30	XM_047439644.1:c.325=	XM_047439644.1:c.325A>T	XM_047439644.1:c.325A>G	XM_047439644.1:c.325A>C
ZNF160 transcript variant X31	XM_047439645.1:c.325=	XM_047439645.1:c.325A>T	XM_047439645.1:c.325A>G	XM_047439645.1:c.325A>C
zinc finger protein 160 isoform X5	XP_016882937.1:p.Lys109=	XP_016882937.1:p.Lys109Ter	XP_016882937.1:p.Lys109Glu	XP_016882937.1:p.Lys109Gln
zinc finger protein 160 isoform X4	XP_016882936.1:p.Lys128=	XP_016882936.1:p.Lys128Ter	XP_016882936.1:p.Lys128Glu	XP_016882936.1:p.Lys128Gln
zinc finger protein 160 isoform c	NP_001309055.1:p.Lys109=	NP_001309055.1:p.Lys109Ter	NP_001309055.1:p.Lys109Glu	NP_001309055.1:p.Lys109Gln
zinc finger protein 160 isoform c	NP_001309054.1:p.Lys109=	NP_001309054.1:p.Lys109Ter	NP_001309054.1:p.Lys109Glu	NP_001309054.1:p.Lys109Gln
zinc finger protein 160 isoform X5	XP_047295599.1:p.Lys109=	XP_047295599.1:p.Lys109Ter	XP_047295599.1:p.Lys109Glu	XP_047295599.1:p.Lys109Gln
zinc finger protein 160 isoform X5	XP_047295602.1:p.Lys109=	XP_047295602.1:p.Lys109Ter	XP_047295602.1:p.Lys109Glu	XP_047295602.1:p.Lys109Gln
zinc finger protein 160 isoform X5	XP_047295600.1:p.Lys109=	XP_047295600.1:p.Lys109Ter	XP_047295600.1:p.Lys109Glu	XP_047295600.1:p.Lys109Gln
zinc finger protein 160 isoform X5	XP_047295601.1:p.Lys109=	XP_047295601.1:p.Lys109Ter	XP_047295601.1:p.Lys109Glu	XP_047295601.1:p.Lys109Gln
ZNF160 transcript variant 3	NM_001102603.1:c.271+684=	NM_001102603.1:c.271+684A>T	NM_001102603.1:c.271+684A>G	NM_001102603.1:c.271+684A>C
ZNF160 transcript variant 3	NM_001102603.2:c.271+684=	NM_001102603.2:c.271+684A>T	NM_001102603.2:c.271+684A>G	NM_001102603.2:c.271+684A>C
ZNF160 transcript variant 4	NM_001322128.2:c.271+684=	NM_001322128.2:c.271+684A>T	NM_001322128.2:c.271+684A>G	NM_001322128.2:c.271+684A>C
ZNF160 transcript variant 5	NM_001322129.2:c.271+684=	NM_001322129.2:c.271+684A>T	NM_001322129.2:c.271+684A>G	NM_001322129.2:c.271+684A>C
ZNF160 transcript variant 6	NM_001322130.2:c.271+684=	NM_001322130.2:c.271+684A>T	NM_001322130.2:c.271+684A>G	NM_001322130.2:c.271+684A>C
ZNF160 transcript variant 7	NM_001322131.2:c.271+684=	NM_001322131.2:c.271+684A>T	NM_001322131.2:c.271+684A>G	NM_001322131.2:c.271+684A>C
ZNF160 transcript variant 8	NM_001322132.2:c.271+684=	NM_001322132.2:c.271+684A>T	NM_001322132.2:c.271+684A>G	NM_001322132.2:c.271+684A>C
ZNF160 transcript variant 9	NM_001322133.2:c.271+684=	NM_001322133.2:c.271+684A>T	NM_001322133.2:c.271+684A>G	NM_001322133.2:c.271+684A>C
ZNF160 transcript variant 10	NM_001322134.2:c.271+684=	NM_001322134.2:c.271+684A>T	NM_001322134.2:c.271+684A>G	NM_001322134.2:c.271+684A>C
ZNF160 transcript variant 11	NM_001322135.2:c.271+684=	NM_001322135.2:c.271+684A>T	NM_001322135.2:c.271+684A>G	NM_001322135.2:c.271+684A>C
ZNF160 transcript variant 12	NM_001322136.1:c.271+684=	NM_001322136.1:c.271+684A>T	NM_001322136.1:c.271+684A>G	NM_001322136.1:c.271+684A>C
ZNF160 transcript variant 13	NM_001322137.2:c.163+684=	NM_001322137.2:c.163+684A>T	NM_001322137.2:c.163+684A>G	NM_001322137.2:c.163+684A>C
ZNF160 transcript variant 14	NM_001322138.2:c.163+684=	NM_001322138.2:c.163+684A>T	NM_001322138.2:c.163+684A>G	NM_001322138.2:c.163+684A>C
ZNF160 transcript variant 15	NM_001322139.2:c.163+684=	NM_001322139.2:c.163+684A>T	NM_001322139.2:c.163+684A>G	NM_001322139.2:c.163+684A>C
ZNF160 transcript variant 1	NM_033288.3:c.271+684=	NM_033288.3:c.271+684A>T	NM_033288.3:c.271+684A>G	NM_033288.3:c.271+684A>C
ZNF160 transcript variant 1	NM_033288.4:c.271+684=	NM_033288.4:c.271+684A>T	NM_033288.4:c.271+684A>G	NM_033288.4:c.271+684A>C
ZNF160 transcript variant 2	NM_198893.2:c.271+684=	NM_198893.2:c.271+684A>T	NM_198893.2:c.271+684A>G	NM_198893.2:c.271+684A>C
ZNF160 transcript variant 2	NM_198893.3:c.271+684=	NM_198893.3:c.271+684A>T	NM_198893.3:c.271+684A>G	NM_198893.3:c.271+684A>C
ZNF160 transcript variant X1	XM_005259378.1:c.271+684=	XM_005259378.1:c.271+684A>T	XM_005259378.1:c.271+684A>G	XM_005259378.1:c.271+684A>C
ZNF160 transcript variant X2	XM_005259379.1:c.163+684=	XM_005259379.1:c.163+684A>T	XM_005259379.1:c.163+684A>G	XM_005259379.1:c.163+684A>C
ZNF160 transcript variant X3	XM_005259380.1:c.328+684=	XM_005259380.1:c.328+684A>T	XM_005259380.1:c.328+684A>G	XM_005259380.1:c.328+684A>C
ZNF160 transcript variant X1	XM_047439616.1:c.271+684=	XM_047439616.1:c.271+684A>T	XM_047439616.1:c.271+684A>G	XM_047439616.1:c.271+684A>C
ZNF160 transcript variant X2	XM_047439617.1:c.328+684=	XM_047439617.1:c.328+684A>T	XM_047439617.1:c.328+684A>G	XM_047439617.1:c.328+684A>C
ZNF160 transcript variant X3	XM_047439618.1:c.271+684=	XM_047439618.1:c.271+684A>T	XM_047439618.1:c.271+684A>G	XM_047439618.1:c.271+684A>C
ZNF160 transcript variant X4	XM_047439619.1:c.271+684=	XM_047439619.1:c.271+684A>T	XM_047439619.1:c.271+684A>G	XM_047439619.1:c.271+684A>C
ZNF160 transcript variant X5	XM_047439620.1:c.271+684=	XM_047439620.1:c.271+684A>T	XM_047439620.1:c.271+684A>G	XM_047439620.1:c.271+684A>C
ZNF160 transcript variant X6	XM_047439621.1:c.271+684=	XM_047439621.1:c.271+684A>T	XM_047439621.1:c.271+684A>G	XM_047439621.1:c.271+684A>C
ZNF160 transcript variant X7	XM_047439622.1:c.271+684=	XM_047439622.1:c.271+684A>T	XM_047439622.1:c.271+684A>G	XM_047439622.1:c.271+684A>C
ZNF160 transcript variant X8	XM_047439623.1:c.271+684=	XM_047439623.1:c.271+684A>T	XM_047439623.1:c.271+684A>G	XM_047439623.1:c.271+684A>C
ZNF160 transcript variant X9	XM_047439624.1:c.328+684=	XM_047439624.1:c.328+684A>T	XM_047439624.1:c.328+684A>G	XM_047439624.1:c.328+684A>C
ZNF160 transcript variant X10	XM_047439625.1:c.163+684=	XM_047439625.1:c.163+684A>T	XM_047439625.1:c.163+684A>G	XM_047439625.1:c.163+684A>C
ZNF160 transcript variant X11	XM_047439626.1:c.163+684=	XM_047439626.1:c.163+684A>T	XM_047439626.1:c.163+684A>G	XM_047439626.1:c.163+684A>C
ZNF160 transcript variant X12	XM_047439627.1:c.163+684=	XM_047439627.1:c.163+684A>T	XM_047439627.1:c.163+684A>G	XM_047439627.1:c.163+684A>C
ZNF160 transcript variant X13	XM_047439628.1:c.163+684=	XM_047439628.1:c.163+684A>T	XM_047439628.1:c.163+684A>G	XM_047439628.1:c.163+684A>C
ZNF160 transcript variant X14	XM_047439629.1:c.163+684=	XM_047439629.1:c.163+684A>T	XM_047439629.1:c.163+684A>G	XM_047439629.1:c.163+684A>C
ZNF160 transcript variant X15	XM_047439630.1:c.163+684=	XM_047439630.1:c.163+684A>T	XM_047439630.1:c.163+684A>G	XM_047439630.1:c.163+684A>C
ZNF160 transcript variant X16	XM_047439631.1:c.163+684=	XM_047439631.1:c.163+684A>T	XM_047439631.1:c.163+684A>G	XM_047439631.1:c.163+684A>C
ZNF160 transcript variant X17	XM_047439632.1:c.163+684=	XM_047439632.1:c.163+684A>T	XM_047439632.1:c.163+684A>G	XM_047439632.1:c.163+684A>C
ZNF160 transcript variant X18	XM_047439633.1:c.163+684=	XM_047439633.1:c.163+684A>T	XM_047439633.1:c.163+684A>G	XM_047439633.1:c.163+684A>C
ZNF160 transcript variant X19	XM_047439634.1:c.163+684=	XM_047439634.1:c.163+684A>T	XM_047439634.1:c.163+684A>G	XM_047439634.1:c.163+684A>C
ZNF160 transcript variant X20	XM_047439635.1:c.163+684=	XM_047439635.1:c.163+684A>T	XM_047439635.1:c.163+684A>G	XM_047439635.1:c.163+684A>C
ZNF160 transcript variant X21	XM_047439636.1:c.163+684=	XM_047439636.1:c.163+684A>T	XM_047439636.1:c.163+684A>G	XM_047439636.1:c.163+684A>C
ZNF160 transcript variant X22	XM_047439637.1:c.163+684=	XM_047439637.1:c.163+684A>T	XM_047439637.1:c.163+684A>G	XM_047439637.1:c.163+684A>C
ZNF160 transcript variant X23	XM_047439638.1:c.163+684=	XM_047439638.1:c.163+684A>T	XM_047439638.1:c.163+684A>G	XM_047439638.1:c.163+684A>C
ZNF160 transcript variant X24	XM_047439639.1:c.163+684=	XM_047439639.1:c.163+684A>T	XM_047439639.1:c.163+684A>G	XM_047439639.1:c.163+684A>C
ZNF160 transcript variant X25	XM_047439640.1:c.163+684=	XM_047439640.1:c.163+684A>T	XM_047439640.1:c.163+684A>G	XM_047439640.1:c.163+684A>C
ZNF160 transcript variant X26	XM_047439641.1:c.163+684=	XM_047439641.1:c.163+684A>T	XM_047439641.1:c.163+684A>G	XM_047439641.1:c.163+684A>C
ZNF160 transcript variant X27	XM_047439642.1:c.163+684=	XM_047439642.1:c.163+684A>T	XM_047439642.1:c.163+684A>G	XM_047439642.1:c.163+684A>C

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#.

4 SubSNP, 4 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss2744275036	Nov 08, 2017 (151)
2	AFFY	ss2985152275	Nov 08, 2017 (151)
3	KOGIC	ss3981591680	Apr 27, 2020 (154)
4	TOPMED	ss5078250266	Apr 27, 2021 (155)
5	gnomAD - Exomes	NC_000019.9 - 53576709	Jul 13, 2019 (153)
6	Korean Genome Project	NC_000019.10 - 53073456	Apr 27, 2020 (154)
7	TopMed	NC_000019.10 - 53073456	Apr 27, 2021 (155)
8	ALFA	NC_000019.10 - 53073456	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
13589731, ss2744275036, ss2985152275	NC_000019.9:53576708:T:A	NC_000019.10:53073455:T:A	(self)
293795930, 1455333455, ss5078250266	NC_000019.10:53073455:T:A	NC_000019.10:53073455:T:A	(self)
1455333455	NC_000019.10:53073455:T:C	NC_000019.10:53073455:T:C	(self)
37969681, ss3981591680	NC_000019.10:53073455:T:G	NC_000019.10:53073455:T:G	(self)

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

No publications for rs1351505374

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1351505374