Variant #0000536292 (NC_000009.11:g.130263438T>C, NC_000009.11(NM_138361.5):c.2046+16T>C (LRSAM1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.130263438T>C
DNA change (hg38) g.127501159T>C
Published as LRSAM1(NM_138361.5):c.2046+16T>C
ISCN -
DB-ID FAM129B_000003 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM129B NM_022833.2 -/. - c.*5686A>G r.(=) p.(=)
LRSAM1 NM_138361.5 -/. - c.2046+16T>C r.(=) p.(=)


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