chr1:94476351:C>T Detail (hg19) (ABCA4)

Information

Genome

Assembly Position
hg19 chr1:94,476,351-94,476,351
hg38 chr1:94,010,795-94,010,795 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000350.2:c.5714+5G>A
Ensemble ENST00000370225.4:c.5714+5G>A
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance Pathogenic Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 601691 OMIM
HGNC 34 HGNC
Ensembl ENSG00000198691 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2024-01-31 criteria provided, multiple submitters, no conflicts not provided germline not provided Detail
Likely pathogenic criteria provided, single submitter retinitis pigmentosa 19 germline Detail
Pathogenic Likely pathogenic 2023-08-01 criteria provided, multiple submitters, no conflicts Severe early-childhood-onset retinal dystrophy germline unknown Detail
Pathogenic 2015-07-23 no assertion criteria provided cone-rod dystrophy 3 germline Detail
Pathogenic 2019-05-08 criteria provided, single submitter Stargardt disease germline inherited unknown Detail
Pathogenic 2018-09-07 criteria provided, single submitter ABCA4-related disorder germline Detail
not provided no assertion provided cone-rod dystrophy,Stargardt disease paternal Detail
not provided no assertion provided cone-rod dystrophy,Stargardt disease paternal Detail
Pathogenic 2019-08-16 criteria provided, single submitter Retinal dystrophy germline Detail
Pathogenic 2019-06-04 criteria provided, single submitter age related macular degeneration 2 unknown Detail
Likely pathogenic 2021-01-30 criteria provided, single submitter Severe early-childhood-onset retinal dystrophy unknown Detail
Pathogenic 2022-01-04 criteria provided, single submitter age related macular degeneration 2,Severe early-childhood-onset retinal dystrophy,cone-rod dystrophy 3,retinitis pigmentosa 19 unknown Detail
Pathogenic 2022-01-04 criteria provided, single submitter age related macular degeneration 2,Severe early-childhood-onset retinal dystrophy,cone-rod dystrophy 3,retinitis pigmentosa 19 unknown Detail
Pathogenic 2022-01-04 criteria provided, single submitter age related macular degeneration 2,Severe early-childhood-onset retinal dystrophy,cone-rod dystrophy 3,retinitis pigmentosa 19 unknown Detail
Pathogenic 2022-01-04 criteria provided, single submitter age related macular degeneration 2,Severe early-childhood-onset retinal dystrophy,cone-rod dystrophy 3,retinitis pigmentosa 19 unknown Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_000350.3(ABCA4):c.5714+5G>A AND not provided ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND Retinitis pigmentosa 19 ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND Severe early-childhood-onset retinal dystrophy ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND Cone-rod dystrophy 3 ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND Stargardt disease ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND ABCA4-related disorder ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND multiple conditions ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND multiple conditions ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND Retinal dystrophy ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND Age related macular degeneration 2 ClinVar Detail
NM_000350.3(ABCA4):c.[5603A>T;5714+5G>A] AND Severe early-childhood-onset retinal dystrophy ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND multiple conditions ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND multiple conditions ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND multiple conditions ClinVar Detail
NM_000350.3(ABCA4):c.5714+5G>A AND multiple conditions ClinVar Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs61751407 dbSNP
Genome
hg19
Position
chr1:94,476,351-94,476,351
Variant Type
snv
Reference Allele
C
Alternative Allele
T
East Asian Chromosome Counts (ExAC)
8644
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
120772
Allele Counts in All Race (ExAC)
42
Heterozygous Counts in All Race (ExAC)
42
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
3.4776272645977547E-4
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