Name: rs36011321
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.

rs36011321

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:179625488-179625508 (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(A)₈ / del(A)₇ / del(A)₆ / del(…
del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.07429 (804/10822, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HNRNPH1 : 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	10822	AAAAAAAAAAAAAAAAAAAAA=0.92321	AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00065, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAA=0.07429, AAAAAAAAAAAAAAAAAAAAAAA=0.00102, AAAAAAAAAAAAAAAAAAAAAAAA=0.00055, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00028, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.882517	0.030809	0.086674	32
European	Sub	8980	AAAAAAAAAAAAAAAAAAAAA=0.9078	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0008, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0892, AAAAAAAAAAAAAAAAAAAAAAA=0.0012, AAAAAAAAAAAAAAAAAAAAAAAA=0.0007, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.858966	0.037161	0.103873	32
African	Sub	938	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	50	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	888	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	84	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	60	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	80	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	416	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	60	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	264	AAAAAAAAAAAAAAAAAAAAA=0.989	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.011, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	0.977273	0.0	0.022727	0

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
Allele Frequency Aggregator	Total	Global	10822	(A)₂₁=0.92321	del(A)₈=0.00000, del(A)₇=0.00065, del(A)₆=0.00000, del(A)₅=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.07429, dupAA=0.00102, dupAAA=0.00055, dup(A)₄=0.00028, dup(A)₆=0.00000
Allele Frequency Aggregator	European	Sub	8980	(A)₂₁=0.9078	del(A)₈=0.0000, del(A)₇=0.0008, del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0892, dupAA=0.0012, dupAAA=0.0007, dup(A)₄=0.0003, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	938	(A)₂₁=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	416	(A)₂₁=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Other	Sub	264	(A)₂₁=0.989	del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.011, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Asian	Sub	84	(A)₂₁=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	80	(A)₂₁=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	60	(A)₂₁=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₆=0.00

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 5	NC_000005.10:g.179625501_179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625502_179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625503_179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625504_179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625505_179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625506_179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625507_179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625508del
GRCh38.p14 chr 5	NC_000005.10:g.179625508dup
GRCh38.p14 chr 5	NC_000005.10:g.179625507_179625508dup
GRCh38.p14 chr 5	NC_000005.10:g.179625506_179625508dup
GRCh38.p14 chr 5	NC_000005.10:g.179625505_179625508dup
GRCh38.p14 chr 5	NC_000005.10:g.179625503_179625508dup
GRCh37.p13 chr 5	NC_000005.9:g.179052502_179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052503_179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052504_179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052505_179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052506_179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052507_179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052508_179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052509del
GRCh37.p13 chr 5	NC_000005.9:g.179052509dup
GRCh37.p13 chr 5	NC_000005.9:g.179052508_179052509dup
GRCh37.p13 chr 5	NC_000005.9:g.179052507_179052509dup
GRCh37.p13 chr 5	NC_000005.9:g.179052506_179052509dup
GRCh37.p13 chr 5	NC_000005.9:g.179052504_179052509dup
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391781_391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391782_391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391783_391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391784_391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391785_391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391786_391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391787_391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391788del
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391788dup
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391787_391788dup
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391786_391788dup
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391785_391788dup
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391783_391788dup

Gene: HNRNPH1, heterogeneous nuclear ribonucleoprotein H1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HNRNPH1 transcript variant 4	NM_001364225.2:c.-169-138… NM_001364225.2:c.-169-1380_-169-1373del	N/A	Intron Variant
HNRNPH1 transcript variant 5	NM_001364226.2:c.-137-129… NM_001364226.2:c.-137-1293_-137-1286del	N/A	Intron Variant
HNRNPH1 transcript variant 12	NM_001364233.2:c.-31-2331… NM_001364233.2:c.-31-2331_-31-2324del	N/A	Intron Variant
HNRNPH1 transcript variant 13	NM_001364234.2:c.-169-138… NM_001364234.2:c.-169-1380_-169-1373del	N/A	Intron Variant
HNRNPH1 transcript variant 14	NM_001364235.2:c.-31-2331… NM_001364235.2:c.-31-2331_-31-2324del	N/A	Intron Variant
HNRNPH1 transcript variant 31	NM_001364253.2:c.-495-233… NM_001364253.2:c.-495-2331_-495-2324del	N/A	Intron Variant
HNRNPH1 transcript variant 50	NM_001395193.1:c.-31-2331… NM_001395193.1:c.-31-2331_-31-2324del	N/A	Intron Variant
HNRNPH1 transcript variant 51	NM_001395194.1:c.-495-233… NM_001395194.1:c.-495-2331_-495-2324del	N/A	Intron Variant
HNRNPH1 transcript variant 1	NM_001257293.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 3	NM_001363572.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 6	NM_001364227.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 7	NM_001364228.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 8	NM_001364229.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 9	NM_001364230.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 10	NM_001364231.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 11	NM_001364232.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 15	NM_001364236.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 16	NM_001364237.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 17	NM_001364238.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 18	NM_001364239.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 19	NM_001364240.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 20	NM_001364241.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 21	NM_001364242.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 22	NM_001364243.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 23	NM_001364244.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 24	NM_001364245.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 25	NM_001364246.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 26	NM_001364247.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 27	NM_001364248.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 28	NM_001364250.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 29	NM_001364251.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 30	NM_001364252.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 32	NM_001364254.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 33	NM_001364255.2:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 34	NM_001395176.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 35	NM_001395177.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 36	NM_001395178.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 37	NM_001395179.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 38	NM_001395180.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 39	NM_001395181.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 40	NM_001395182.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 41	NM_001395183.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 42	NM_001395184.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 43	NM_001395186.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 44	NM_001395187.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 45	NM_001395188.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 46	NM_001395189.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 47	NM_001395190.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 48	NM_001395191.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 49	NM_001395192.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 52	NM_001395195.1:c.	N/A	Genic Upstream Transcript Variant
HNRNPH1 transcript variant 2	NM_005520.3:c.	N/A	Genic Upstream Transcript 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	(A)₂₁=	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆
GRCh38.p14 chr 5	NC_000005.10:g.179625488_179625508=	NC_000005.10:g.179625501_179625508del	NC_000005.10:g.179625502_179625508del	NC_000005.10:g.179625503_179625508del	NC_000005.10:g.179625504_179625508del	NC_000005.10:g.179625505_179625508del	NC_000005.10:g.179625506_179625508del	NC_000005.10:g.179625507_179625508del	NC_000005.10:g.179625508del	NC_000005.10:g.179625508dup	NC_000005.10:g.179625507_179625508dup	NC_000005.10:g.179625506_179625508dup	NC_000005.10:g.179625505_179625508dup	NC_000005.10:g.179625503_179625508dup
GRCh37.p13 chr 5	NC_000005.9:g.179052489_179052509=	NC_000005.9:g.179052502_179052509del	NC_000005.9:g.179052503_179052509del	NC_000005.9:g.179052504_179052509del	NC_000005.9:g.179052505_179052509del	NC_000005.9:g.179052506_179052509del	NC_000005.9:g.179052507_179052509del	NC_000005.9:g.179052508_179052509del	NC_000005.9:g.179052509del	NC_000005.9:g.179052509dup	NC_000005.9:g.179052508_179052509dup	NC_000005.9:g.179052507_179052509dup	NC_000005.9:g.179052506_179052509dup	NC_000005.9:g.179052504_179052509dup
GRCh38.p14 chr 5 fix patch HG30_PATCH	NW_016107298.1:g.391767_391788=	NW_016107298.1:g.391781_391788del	NW_016107298.1:g.391782_391788del	NW_016107298.1:g.391783_391788del	NW_016107298.1:g.391784_391788del	NW_016107298.1:g.391785_391788del	NW_016107298.1:g.391786_391788del	NW_016107298.1:g.391787_391788del	NW_016107298.1:g.391788del	NW_016107298.1:g.391788dup	NW_016107298.1:g.391787_391788dup	NW_016107298.1:g.391786_391788dup	NW_016107298.1:g.391785_391788dup	NW_016107298.1:g.391783_391788dup
HNRNPH1 transcript variant 4	NM_001364225.2:c.-169-1373=	NM_001364225.2:c.-169-1380_-169-1373del	NM_001364225.2:c.-169-1379_-169-1373del	NM_001364225.2:c.-169-1378_-169-1373del	NM_001364225.2:c.-169-1377_-169-1373del	NM_001364225.2:c.-169-1376_-169-1373del	NM_001364225.2:c.-169-1375_-169-1373del	NM_001364225.2:c.-169-1374_-169-1373del	NM_001364225.2:c.-169-1373del	NM_001364225.2:c.-169-1373dup	NM_001364225.2:c.-169-1374_-169-1373dup	NM_001364225.2:c.-169-1375_-169-1373dup	NM_001364225.2:c.-169-1376_-169-1373dup	NM_001364225.2:c.-169-1378_-169-1373dup
HNRNPH1 transcript variant 5	NM_001364226.2:c.-137-1286=	NM_001364226.2:c.-137-1293_-137-1286del	NM_001364226.2:c.-137-1292_-137-1286del	NM_001364226.2:c.-137-1291_-137-1286del	NM_001364226.2:c.-137-1290_-137-1286del	NM_001364226.2:c.-137-1289_-137-1286del	NM_001364226.2:c.-137-1288_-137-1286del	NM_001364226.2:c.-137-1287_-137-1286del	NM_001364226.2:c.-137-1286del	NM_001364226.2:c.-137-1286dup	NM_001364226.2:c.-137-1287_-137-1286dup	NM_001364226.2:c.-137-1288_-137-1286dup	NM_001364226.2:c.-137-1289_-137-1286dup	NM_001364226.2:c.-137-1291_-137-1286dup
HNRNPH1 transcript variant 12	NM_001364233.2:c.-31-2324=	NM_001364233.2:c.-31-2331_-31-2324del	NM_001364233.2:c.-31-2330_-31-2324del	NM_001364233.2:c.-31-2329_-31-2324del	NM_001364233.2:c.-31-2328_-31-2324del	NM_001364233.2:c.-31-2327_-31-2324del	NM_001364233.2:c.-31-2326_-31-2324del	NM_001364233.2:c.-31-2325_-31-2324del	NM_001364233.2:c.-31-2324del	NM_001364233.2:c.-31-2324dup	NM_001364233.2:c.-31-2325_-31-2324dup	NM_001364233.2:c.-31-2326_-31-2324dup	NM_001364233.2:c.-31-2327_-31-2324dup	NM_001364233.2:c.-31-2329_-31-2324dup
HNRNPH1 transcript variant 13	NM_001364234.2:c.-169-1373=	NM_001364234.2:c.-169-1380_-169-1373del	NM_001364234.2:c.-169-1379_-169-1373del	NM_001364234.2:c.-169-1378_-169-1373del	NM_001364234.2:c.-169-1377_-169-1373del	NM_001364234.2:c.-169-1376_-169-1373del	NM_001364234.2:c.-169-1375_-169-1373del	NM_001364234.2:c.-169-1374_-169-1373del	NM_001364234.2:c.-169-1373del	NM_001364234.2:c.-169-1373dup	NM_001364234.2:c.-169-1374_-169-1373dup	NM_001364234.2:c.-169-1375_-169-1373dup	NM_001364234.2:c.-169-1376_-169-1373dup	NM_001364234.2:c.-169-1378_-169-1373dup
HNRNPH1 transcript variant 14	NM_001364235.2:c.-31-2324=	NM_001364235.2:c.-31-2331_-31-2324del	NM_001364235.2:c.-31-2330_-31-2324del	NM_001364235.2:c.-31-2329_-31-2324del	NM_001364235.2:c.-31-2328_-31-2324del	NM_001364235.2:c.-31-2327_-31-2324del	NM_001364235.2:c.-31-2326_-31-2324del	NM_001364235.2:c.-31-2325_-31-2324del	NM_001364235.2:c.-31-2324del	NM_001364235.2:c.-31-2324dup	NM_001364235.2:c.-31-2325_-31-2324dup	NM_001364235.2:c.-31-2326_-31-2324dup	NM_001364235.2:c.-31-2327_-31-2324dup	NM_001364235.2:c.-31-2329_-31-2324dup
HNRNPH1 transcript variant 31	NM_001364253.2:c.-495-2324=	NM_001364253.2:c.-495-2331_-495-2324del	NM_001364253.2:c.-495-2330_-495-2324del	NM_001364253.2:c.-495-2329_-495-2324del	NM_001364253.2:c.-495-2328_-495-2324del	NM_001364253.2:c.-495-2327_-495-2324del	NM_001364253.2:c.-495-2326_-495-2324del	NM_001364253.2:c.-495-2325_-495-2324del	NM_001364253.2:c.-495-2324del	NM_001364253.2:c.-495-2324dup	NM_001364253.2:c.-495-2325_-495-2324dup	NM_001364253.2:c.-495-2326_-495-2324dup	NM_001364253.2:c.-495-2327_-495-2324dup	NM_001364253.2:c.-495-2329_-495-2324dup
HNRNPH1 transcript variant 50	NM_001395193.1:c.-31-2324=	NM_001395193.1:c.-31-2331_-31-2324del	NM_001395193.1:c.-31-2330_-31-2324del	NM_001395193.1:c.-31-2329_-31-2324del	NM_001395193.1:c.-31-2328_-31-2324del	NM_001395193.1:c.-31-2327_-31-2324del	NM_001395193.1:c.-31-2326_-31-2324del	NM_001395193.1:c.-31-2325_-31-2324del	NM_001395193.1:c.-31-2324del	NM_001395193.1:c.-31-2324dup	NM_001395193.1:c.-31-2325_-31-2324dup	NM_001395193.1:c.-31-2326_-31-2324dup	NM_001395193.1:c.-31-2327_-31-2324dup	NM_001395193.1:c.-31-2329_-31-2324dup
HNRNPH1 transcript variant 51	NM_001395194.1:c.-495-2324=	NM_001395194.1:c.-495-2331_-495-2324del	NM_001395194.1:c.-495-2330_-495-2324del	NM_001395194.1:c.-495-2329_-495-2324del	NM_001395194.1:c.-495-2328_-495-2324del	NM_001395194.1:c.-495-2327_-495-2324del	NM_001395194.1:c.-495-2326_-495-2324del	NM_001395194.1:c.-495-2325_-495-2324del	NM_001395194.1:c.-495-2324del	NM_001395194.1:c.-495-2324dup	NM_001395194.1:c.-495-2325_-495-2324dup	NM_001395194.1:c.-495-2326_-495-2324dup	NM_001395194.1:c.-495-2327_-495-2324dup	NM_001395194.1:c.-495-2329_-495-2324dup

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#.

30 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42468645	Mar 15, 2006 (126)
2	SWEGEN	ss2998350061	Nov 08, 2017 (151)
3	MCHAISSO	ss3065064073	Nov 08, 2017 (151)
4	EVA	ss3829676645	Apr 26, 2020 (154)
5	GNOMAD	ss4135277971	Apr 26, 2021 (155)
6	GNOMAD	ss4135277972	Apr 26, 2021 (155)
7	GNOMAD	ss4135277973	Apr 26, 2021 (155)
8	GNOMAD	ss4135277974	Apr 26, 2021 (155)
9	GNOMAD	ss4135277975	Apr 26, 2021 (155)
10	GNOMAD	ss4135277976	Apr 26, 2021 (155)
11	GNOMAD	ss4135277977	Apr 26, 2021 (155)
12	GNOMAD	ss4135277978	Apr 26, 2021 (155)
13	GNOMAD	ss4135277979	Apr 26, 2021 (155)
14	GNOMAD	ss4135277980	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5175705149	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5175705150	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5175705151	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5175705152	Apr 26, 2021 (155)
19	1000G_HIGH_COVERAGE	ss5267048406	Oct 13, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5267048407	Oct 13, 2022 (156)
21	1000G_HIGH_COVERAGE	ss5267048408	Oct 13, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5267048409	Oct 13, 2022 (156)
23	HUGCELL_USP	ss5464880461	Oct 13, 2022 (156)
24	HUGCELL_USP	ss5464880462	Oct 13, 2022 (156)
25	HUGCELL_USP	ss5464880463	Oct 13, 2022 (156)
26	TOMMO_GENOMICS	ss5713236497	Oct 13, 2022 (156)
27	TOMMO_GENOMICS	ss5713236498	Oct 13, 2022 (156)
28	TOMMO_GENOMICS	ss5713236499	Oct 13, 2022 (156)
29	TOMMO_GENOMICS	ss5713236500	Oct 13, 2022 (156)
30	TOMMO_GENOMICS	ss5713236501	Oct 13, 2022 (156)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214312010 (NC_000005.10:179625487::A 23723/78732) Row 214312011 (NC_000005.10:179625487::AA 1070/78814) Row 214312012 (NC_000005.10:179625487::AAA 11/78848)...	-	Apr 26, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 33674456 (NC_000005.9:179052488::A 1854/16688) Row 33674457 (NC_000005.9:179052488::AA 24/16688) Row 33674458 (NC_000005.9:179052488:A: 18/16688)...	-	Apr 26, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 33674456 (NC_000005.9:179052488::A 1854/16688) Row 33674457 (NC_000005.9:179052488::AA 24/16688) Row 33674458 (NC_000005.9:179052488:A: 18/16688)...	-	Apr 26, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 33674456 (NC_000005.9:179052488::A 1854/16688) Row 33674457 (NC_000005.9:179052488::AA 24/16688) Row 33674458 (NC_000005.9:179052488:A: 18/16688)...	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 33674456 (NC_000005.9:179052488::A 1854/16688) Row 33674457 (NC_000005.9:179052488::AA 24/16688) Row 33674458 (NC_000005.9:179052488:A: 18/16688)...	-	Apr 26, 2021 (155)
45	14KJPN Submission ignored due to conflicting rows: Row 47073601 (NC_000005.10:179625487::A 2940/28012) Row 47073602 (NC_000005.10:179625487::AA 28/28012) Row 47073603 (NC_000005.10:179625487:AAAAAA: 2/28012)...	-	Oct 13, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 47073601 (NC_000005.10:179625487::A 2940/28012) Row 47073602 (NC_000005.10:179625487::AA 28/28012) Row 47073603 (NC_000005.10:179625487:AAAAAA: 2/28012)...	-	Oct 13, 2022 (156)
47	14KJPN Submission ignored due to conflicting rows: Row 47073601 (NC_000005.10:179625487::A 2940/28012) Row 47073602 (NC_000005.10:179625487::AA 28/28012) Row 47073603 (NC_000005.10:179625487:AAAAAA: 2/28012)...	-	Oct 13, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 47073601 (NC_000005.10:179625487::A 2940/28012) Row 47073602 (NC_000005.10:179625487::AA 28/28012) Row 47073603 (NC_000005.10:179625487:AAAAAA: 2/28012)...	-	Oct 13, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 47073601 (NC_000005.10:179625487::A 2940/28012) Row 47073602 (NC_000005.10:179625487::AA 28/28012) Row 47073603 (NC_000005.10:179625487:AAAAAA: 2/28012)...	-	Oct 13, 2022 (156)
50	ALFA	NC_000005.10 - 179625488	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4135277980	NC_000005.10:179625487:AAAAAAAA:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss2998350061	NC_000005.9:179052488:AAAAAAA:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4135277979, ss5267048409, ss5464880463	NC_000005.10:179625487:AAAAAAA:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4135277978, ss5713236499	NC_000005.10:179625487:AAAAAA:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4135277977	NC_000005.10:179625487:AAAA:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4135277976	NC_000005.10:179625487:AA:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5175705151	NC_000005.9:179052488:A:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4135277975, ss5267048408, ss5464880462, ss5713236500	NC_000005.10:179625487:A:	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3829676645, ss5175705149	NC_000005.9:179052488::A	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3065064073, ss4135277971, ss5267048406, ss5464880461, ss5713236497	NC_000005.10:179625487::A	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss42468645	NT_023133.13:23863761::A	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5175705150	NC_000005.9:179052488::AA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4135277972, ss5267048407, ss5713236498	NC_000005.10:179625487::AA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4135277973	NC_000005.10:179625487::AAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5175705152	NC_000005.9:179052488::AAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5713236501	NC_000005.10:179625487::AAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4135277974	NC_000005.10:179625487::AAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
14187350954	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:179625487:AAAAAAAAAAA… NC_000005.10:179625487:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs36011321

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs36011321