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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1467301764

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr19:53108885 (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>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000004 (1/251264, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ZNF415 : Missense Variant
Publications
0 citations
Genomic View
See rs on genome
Help

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
gnomAD - Exomes Global Study-wide 251264 T=0.999996 C=0.000004
gnomAD - Exomes European Sub 135252 T=0.999993 C=0.000007
gnomAD - Exomes Asian Sub 48996 T=1.00000 C=0.00000
gnomAD - Exomes American Sub 34568 T=1.00000 C=0.00000
gnomAD - Exomes African Sub 16244 T=1.00000 C=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10080 T=1.00000 C=0.00000
gnomAD - Exomes Other Sub 6124 T=1.0000 C=0.0000
Help

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.53108885T>C
GRCh37.p13 chr 19 NC_000019.9:g.53612138T>C
Gene: ZNF415, zinc finger protein 415 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ZNF415 transcript variant 6 NM_001352130.2:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 5 NP_001339059.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 19 NM_001352143.2:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 1 NP_001339072.1:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 13 NM_001352137.2:c.1268A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 7 NP_001339066.1:p.Asn423Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 17 NM_001352141.2:c.1196A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 8 NP_001339070.1:p.Asn399Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 25 NM_001352150.2:c.470A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 4 NP_001339079.1:p.Asn157Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 1 NM_001136038.4:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 1 NP_001129510.2:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 24 NM_001352149.2:c.1121A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 9 NP_001339078.1:p.Asn374Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 4 NM_001330766.2:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 3 NP_001317695.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 12 NM_001352136.2:c.1268A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 7 NP_001339065.1:p.Asn423Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 15 NM_001352139.2:c.1196A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 8 NP_001339068.1:p.Asn399Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 23 NM_001352148.2:c.1121A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 9 NP_001339077.1:p.Asn374Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 18 NM_001352142.2:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 1 NP_001339071.1:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 22 NM_001352147.2:c.1121A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 9 NP_001339076.1:p.Asn374Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 26 NM_001352151.2:c.470A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 4 NP_001339080.1:p.Asn157Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 10 NM_001352134.2:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 3 NP_001339063.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 5 NM_001330759.2:c.470A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 4 NP_001317688.1:p.Asn157Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 14 NM_001352138.2:c.1196A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 8 NP_001339067.1:p.Asn399Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 2 NM_018355.4:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 2 NP_060825.2:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 8 NM_001352132.2:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 3 NP_001339061.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 16 NM_001352140.2:c.1196A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 8 NP_001339069.1:p.Asn399Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 11 NM_001352135.2:c.1298A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 6 NP_001339064.1:p.Asn433Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 9 NM_001352133.2:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 3 NP_001339062.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 21 NM_001352146.2:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 2 NP_001339075.1:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 3 NM_001164309.3:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 2 NP_001157781.1:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 7 NM_001352131.2:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 5 NP_001339060.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant 20 NM_001352144.2:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform 1 NP_001339073.1:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X22 XM_047439091.1:c. N/A Genic Downstream Transcript Variant
ZNF415 transcript variant X1 XM_047439079.1:c.1631A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X1 XP_047295035.1:p.Asn544Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X2 XM_024451595.2:c.1529A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X2 XP_024307363.1:p.Asn510Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X3 XM_047439080.1:c.1508A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X3 XP_047295036.1:p.Asn503Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X4 XM_047439081.1:c.1400A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X4 XP_047295037.1:p.Asn467Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X5 XM_024451596.2:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X5 XP_024307364.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X6 XM_006723267.2:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X5 XP_006723330.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X7 XM_024451597.2:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X5 XP_024307365.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X8 XM_024451598.2:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X5 XP_024307366.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X9 XM_024451599.2:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X5 XP_024307367.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X10 XM_047439082.1:c.1391A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X5 XP_047295038.1:p.Asn464Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X11 XM_047439083.1:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X6 XP_047295039.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X12 XM_047439084.1:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X6 XP_047295040.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X13 XM_047439085.1:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X6 XP_047295041.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X14 XM_017026960.2:c.1304A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X6 XP_016882449.1:p.Asn435Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X15 XM_047439086.1:c.1274A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X7 XP_047295042.1:p.Asn425Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X16 XM_047439087.1:c.1268A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X8 XP_047295043.1:p.Asn423Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X17 XM_047439088.1:c.1196A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X9 XP_047295044.1:p.Asn399Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X18 XM_017026964.2:c.1160A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X10 XP_016882453.1:p.Asn387Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X19 XM_047439089.1:c.1121A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X11 XP_047295045.1:p.Asn374Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X20 XM_017026969.2:c.1073A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X12 XP_016882458.1:p.Asn358Ser N (Asn) > S (Ser) Missense Variant
ZNF415 transcript variant X21 XM_047439090.1:c.1058A>G N [AAT] > S [AGT] Coding Sequence Variant
zinc finger protein 415 isoform X13 XP_047295046.1:p.Asn353Ser N (Asn) > S (Ser) Missense Variant
Help

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
Help

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= C
GRCh38.p14 chr 19 NC_000019.10:g.53108885= NC_000019.10:g.53108885T>C
GRCh37.p13 chr 19 NC_000019.9:g.53612138= NC_000019.9:g.53612138T>C
ZNF415 transcript variant 1 NM_001136038.4:c.1160= NM_001136038.4:c.1160A>G
ZNF415 transcript variant 1 NM_001136038.3:c.1160= NM_001136038.3:c.1160A>G
ZNF415 transcript variant 1 NM_001136038.2:c.1160= NM_001136038.2:c.1160A>G
ZNF415 transcript variant 2 NM_018355.4:c.1160= NM_018355.4:c.1160A>G
ZNF415 transcript variant 2 NM_018355.3:c.1160= NM_018355.3:c.1160A>G
ZNF415 transcript variant 3 NM_001164309.3:c.1160= NM_001164309.3:c.1160A>G
ZNF415 transcript variant 3 NM_001164309.2:c.1160= NM_001164309.2:c.1160A>G
ZNF415 transcript variant 3 NM_001164309.1:c.1160= NM_001164309.1:c.1160A>G
ZNF415 transcript variant X5 XM_024451596.2:c.1391= XM_024451596.2:c.1391A>G
ZNF415 transcript variant X3 XM_024451596.1:c.1391= XM_024451596.1:c.1391A>G
ZNF415 transcript variant 6 NM_001352130.2:c.1391= NM_001352130.2:c.1391A>G
ZNF415 transcript variant 6 NM_001352130.1:c.1391= NM_001352130.1:c.1391A>G
ZNF415 transcript variant 23 NM_001352148.2:c.1121= NM_001352148.2:c.1121A>G
ZNF415 transcript variant 23 NM_001352148.1:c.1121= NM_001352148.1:c.1121A>G
ZNF415 transcript variant 9 NM_001352133.2:c.1304= NM_001352133.2:c.1304A>G
ZNF415 transcript variant 9 NM_001352133.1:c.1304= NM_001352133.1:c.1304A>G
ZNF415 transcript variant X8 XM_024451598.2:c.1391= XM_024451598.2:c.1391A>G
ZNF415 transcript variant X5 XM_024451598.1:c.1391= XM_024451598.1:c.1391A>G
ZNF415 transcript variant 20 NM_001352144.2:c.1160= NM_001352144.2:c.1160A>G
ZNF415 transcript variant 20 NM_001352144.1:c.1160= NM_001352144.1:c.1160A>G
ZNF415 transcript variant X9 XM_024451599.2:c.1391= XM_024451599.2:c.1391A>G
ZNF415 transcript variant X6 XM_024451599.1:c.1391= XM_024451599.1:c.1391A>G
ZNF415 transcript variant 24 NM_001352149.2:c.1121= NM_001352149.2:c.1121A>G
ZNF415 transcript variant 24 NM_001352149.1:c.1121= NM_001352149.1:c.1121A>G
ZNF415 transcript variant 4 NM_001330766.2:c.1304= NM_001330766.2:c.1304A>G
ZNF415 transcript variant 4 NM_001330766.1:c.1304= NM_001330766.1:c.1304A>G
ZNF415 transcript variant 7 NM_001352131.2:c.1391= NM_001352131.2:c.1391A>G
ZNF415 transcript variant 7 NM_001352131.1:c.1391= NM_001352131.1:c.1391A>G
ZNF415 transcript variant 13 NM_001352137.2:c.1268= NM_001352137.2:c.1268A>G
ZNF415 transcript variant 13 NM_001352137.1:c.1268= NM_001352137.1:c.1268A>G
ZNF415 transcript variant X6 XM_006723267.2:c.1391= XM_006723267.2:c.1391A>G
ZNF415 transcript variant X2 XM_006723267.1:c.1391= XM_006723267.1:c.1391A>G
ZNF415 transcript variant 8 NM_001352132.2:c.1304= NM_001352132.2:c.1304A>G
ZNF415 transcript variant 8 NM_001352132.1:c.1304= NM_001352132.1:c.1304A>G
ZNF415 transcript variant 17 NM_001352141.2:c.1196= NM_001352141.2:c.1196A>G
ZNF415 transcript variant 17 NM_001352141.1:c.1196= NM_001352141.1:c.1196A>G
ZNF415 transcript variant 10 NM_001352134.2:c.1304= NM_001352134.2:c.1304A>G
ZNF415 transcript variant 10 NM_001352134.1:c.1304= NM_001352134.1:c.1304A>G
ZNF415 transcript variant X2 XM_024451595.2:c.1529= XM_024451595.2:c.1529A>G
ZNF415 transcript variant X1 XM_024451595.1:c.1529= XM_024451595.1:c.1529A>G
ZNF415 transcript variant X18 XM_017026964.2:c.1160= XM_017026964.2:c.1160A>G
ZNF415 transcript variant X14 XM_017026964.1:c.1160= XM_017026964.1:c.1160A>G
ZNF415 transcript variant 12 NM_001352136.2:c.1268= NM_001352136.2:c.1268A>G
ZNF415 transcript variant 12 NM_001352136.1:c.1268= NM_001352136.1:c.1268A>G
ZNF415 transcript variant 19 NM_001352143.2:c.1160= NM_001352143.2:c.1160A>G
ZNF415 transcript variant 19 NM_001352143.1:c.1160= NM_001352143.1:c.1160A>G
ZNF415 transcript variant X7 XM_024451597.2:c.1391= XM_024451597.2:c.1391A>G
ZNF415 transcript variant X4 XM_024451597.1:c.1391= XM_024451597.1:c.1391A>G
ZNF415 transcript variant 14 NM_001352138.2:c.1196= NM_001352138.2:c.1196A>G
ZNF415 transcript variant 14 NM_001352138.1:c.1196= NM_001352138.1:c.1196A>G
ZNF415 transcript variant 22 NM_001352147.2:c.1121= NM_001352147.2:c.1121A>G
ZNF415 transcript variant 22 NM_001352147.1:c.1121= NM_001352147.1:c.1121A>G
ZNF415 transcript variant 16 NM_001352140.2:c.1196= NM_001352140.2:c.1196A>G
ZNF415 transcript variant 16 NM_001352140.1:c.1196= NM_001352140.1:c.1196A>G
ZNF415 transcript variant 21 NM_001352146.2:c.1160= NM_001352146.2:c.1160A>G
ZNF415 transcript variant 21 NM_001352146.1:c.1160= NM_001352146.1:c.1160A>G
ZNF415 transcript variant 26 NM_001352151.2:c.470= NM_001352151.2:c.470A>G
ZNF415 transcript variant 26 NM_001352151.1:c.470= NM_001352151.1:c.470A>G
ZNF415 transcript variant 18 NM_001352142.2:c.1160= NM_001352142.2:c.1160A>G
ZNF415 transcript variant 18 NM_001352142.1:c.1160= NM_001352142.1:c.1160A>G
ZNF415 transcript variant X14 XM_017026960.2:c.1304= XM_017026960.2:c.1304A>G
ZNF415 transcript variant X10 XM_017026960.1:c.1304= XM_017026960.1:c.1304A>G
ZNF415 transcript variant 15 NM_001352139.2:c.1196= NM_001352139.2:c.1196A>G
ZNF415 transcript variant 15 NM_001352139.1:c.1196= NM_001352139.1:c.1196A>G
ZNF415 transcript variant 11 NM_001352135.2:c.1298= NM_001352135.2:c.1298A>G
ZNF415 transcript variant 11 NM_001352135.1:c.1298= NM_001352135.1:c.1298A>G
ZNF415 transcript variant 5 NM_001330759.2:c.470= NM_001330759.2:c.470A>G
ZNF415 transcript variant 5 NM_001330759.1:c.470= NM_001330759.1:c.470A>G
ZNF415 transcript variant X20 XM_017026969.2:c.1073= XM_017026969.2:c.1073A>G
ZNF415 transcript variant X18 XM_017026969.1:c.1073= XM_017026969.1:c.1073A>G
ZNF415 transcript variant 25 NM_001352150.2:c.470= NM_001352150.2:c.470A>G
ZNF415 transcript variant 25 NM_001352150.1:c.470= NM_001352150.1:c.470A>G
ZNF415 transcript variant X11 XM_047439083.1:c.1304= XM_047439083.1:c.1304A>G
ZNF415 transcript variant X16 XM_047439087.1:c.1268= XM_047439087.1:c.1268A>G
ZNF415 transcript variant X10 XM_047439082.1:c.1391= XM_047439082.1:c.1391A>G
ZNF415 transcript variant X17 XM_047439088.1:c.1196= XM_047439088.1:c.1196A>G
ZNF415 transcript variant X12 XM_047439084.1:c.1304= XM_047439084.1:c.1304A>G
ZNF415 transcript variant X13 XM_047439085.1:c.1304= XM_047439085.1:c.1304A>G
ZNF415 transcript variant X1 XM_047439079.1:c.1631= XM_047439079.1:c.1631A>G
ZNF415 transcript variant 4 NR_028343.1:n.1653= NR_028343.1:n.1653A>G
ZNF415 transcript variant X3 XM_047439080.1:c.1508= XM_047439080.1:c.1508A>G
ZNF415 transcript variant X15 XM_047439086.1:c.1274= XM_047439086.1:c.1274A>G
ZNF415 transcript variant X4 XM_047439081.1:c.1400= XM_047439081.1:c.1400A>G
ZNF415 transcript variant X19 XM_047439089.1:c.1121= XM_047439089.1:c.1121A>G
ZNF415 transcript variant X21 XM_047439090.1:c.1058= XM_047439090.1:c.1058A>G
zinc finger protein 415 isoform 1 NP_001129510.2:p.Asn387= NP_001129510.2:p.Asn387Ser
zinc finger protein 415 isoform 2 NP_060825.2:p.Asn387= NP_060825.2:p.Asn387Ser
zinc finger protein 415 isoform 2 NP_001157781.1:p.Asn387= NP_001157781.1:p.Asn387Ser
zinc finger protein 415 isoform X5 XP_024307364.1:p.Asn464= XP_024307364.1:p.Asn464Ser
zinc finger protein 415 isoform 5 NP_001339059.1:p.Asn464= NP_001339059.1:p.Asn464Ser
zinc finger protein 415 isoform 9 NP_001339077.1:p.Asn374= NP_001339077.1:p.Asn374Ser
zinc finger protein 415 isoform 3 NP_001339062.1:p.Asn435= NP_001339062.1:p.Asn435Ser
zinc finger protein 415 isoform X5 XP_024307366.1:p.Asn464= XP_024307366.1:p.Asn464Ser
zinc finger protein 415 isoform 1 NP_001339073.1:p.Asn387= NP_001339073.1:p.Asn387Ser
zinc finger protein 415 isoform X5 XP_024307367.1:p.Asn464= XP_024307367.1:p.Asn464Ser
zinc finger protein 415 isoform 9 NP_001339078.1:p.Asn374= NP_001339078.1:p.Asn374Ser
zinc finger protein 415 isoform 3 NP_001317695.1:p.Asn435= NP_001317695.1:p.Asn435Ser
zinc finger protein 415 isoform 5 NP_001339060.1:p.Asn464= NP_001339060.1:p.Asn464Ser
zinc finger protein 415 isoform 7 NP_001339066.1:p.Asn423= NP_001339066.1:p.Asn423Ser
zinc finger protein 415 isoform X5 XP_006723330.1:p.Asn464= XP_006723330.1:p.Asn464Ser
zinc finger protein 415 isoform 3 NP_001339061.1:p.Asn435= NP_001339061.1:p.Asn435Ser
zinc finger protein 415 isoform 8 NP_001339070.1:p.Asn399= NP_001339070.1:p.Asn399Ser
zinc finger protein 415 isoform 3 NP_001339063.1:p.Asn435= NP_001339063.1:p.Asn435Ser
zinc finger protein 415 isoform X2 XP_024307363.1:p.Asn510= XP_024307363.1:p.Asn510Ser
zinc finger protein 415 isoform X10 XP_016882453.1:p.Asn387= XP_016882453.1:p.Asn387Ser
zinc finger protein 415 isoform 7 NP_001339065.1:p.Asn423= NP_001339065.1:p.Asn423Ser
zinc finger protein 415 isoform 1 NP_001339072.1:p.Asn387= NP_001339072.1:p.Asn387Ser
zinc finger protein 415 isoform X5 XP_024307365.1:p.Asn464= XP_024307365.1:p.Asn464Ser
zinc finger protein 415 isoform 8 NP_001339067.1:p.Asn399= NP_001339067.1:p.Asn399Ser
zinc finger protein 415 isoform 9 NP_001339076.1:p.Asn374= NP_001339076.1:p.Asn374Ser
zinc finger protein 415 isoform 8 NP_001339069.1:p.Asn399= NP_001339069.1:p.Asn399Ser
zinc finger protein 415 isoform 2 NP_001339075.1:p.Asn387= NP_001339075.1:p.Asn387Ser
zinc finger protein 415 isoform 4 NP_001339080.1:p.Asn157= NP_001339080.1:p.Asn157Ser
zinc finger protein 415 isoform 1 NP_001339071.1:p.Asn387= NP_001339071.1:p.Asn387Ser
zinc finger protein 415 isoform X6 XP_016882449.1:p.Asn435= XP_016882449.1:p.Asn435Ser
zinc finger protein 415 isoform 8 NP_001339068.1:p.Asn399= NP_001339068.1:p.Asn399Ser
zinc finger protein 415 isoform 6 NP_001339064.1:p.Asn433= NP_001339064.1:p.Asn433Ser
zinc finger protein 415 isoform 4 NP_001317688.1:p.Asn157= NP_001317688.1:p.Asn157Ser
zinc finger protein 415 isoform X12 XP_016882458.1:p.Asn358= XP_016882458.1:p.Asn358Ser
zinc finger protein 415 isoform 4 NP_001339079.1:p.Asn157= NP_001339079.1:p.Asn157Ser
zinc finger protein 415 isoform X6 XP_047295039.1:p.Asn435= XP_047295039.1:p.Asn435Ser
zinc finger protein 415 isoform X8 XP_047295043.1:p.Asn423= XP_047295043.1:p.Asn423Ser
zinc finger protein 415 isoform X5 XP_047295038.1:p.Asn464= XP_047295038.1:p.Asn464Ser
zinc finger protein 415 isoform X9 XP_047295044.1:p.Asn399= XP_047295044.1:p.Asn399Ser
zinc finger protein 415 isoform X6 XP_047295040.1:p.Asn435= XP_047295040.1:p.Asn435Ser
zinc finger protein 415 isoform X6 XP_047295041.1:p.Asn435= XP_047295041.1:p.Asn435Ser
zinc finger protein 415 isoform X1 XP_047295035.1:p.Asn544= XP_047295035.1:p.Asn544Ser
zinc finger protein 415 isoform X3 XP_047295036.1:p.Asn503= XP_047295036.1:p.Asn503Ser
zinc finger protein 415 isoform X7 XP_047295042.1:p.Asn425= XP_047295042.1:p.Asn425Ser
zinc finger protein 415 isoform X4 XP_047295037.1:p.Asn467= XP_047295037.1:p.Asn467Ser
zinc finger protein 415 isoform X11 XP_047295045.1:p.Asn374= XP_047295045.1:p.Asn374Ser
zinc finger protein 415 isoform X13 XP_047295046.1:p.Asn353= XP_047295046.1:p.Asn353Ser
Help

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#.

1 SubSNP, 1 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2744275328 Nov 08, 2017 (151)
2 gnomAD - Exomes NC_000019.9 - 53612138 Jul 13, 2019 (153)
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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
13590053, ss2744275328 NC_000019.9:53612137:T:C NC_000019.10:53108884:T:C (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1467301764

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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.

Software version is: 2.0.1.post820+afb47a3d