Version: 8.0.0
Date: Tue Jan 28 2025
14,083 results
Allele/Variant Genes: BRCA2 (Hsa)

(GRCh38)13:32315667G>A

(Homo sapiens)
Allele/Variant
Source: rs1555279967
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315667G>A

(GRCh38)13:32315667G>C

(Homo sapiens)
Allele/Variant
Source: rs1555279967
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315667G>C

(GRCh38)13:32315677G>A

(Homo sapiens)
Allele/Variant
Source: NC_000013.11:g.32315677G>A
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315677G>A

(GRCh38)13:32319099T>C

(Homo sapiens)
Allele/Variant
Source: rs760655471
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319099T>C

(GRCh38)13:32319174C>T

(Homo sapiens)
Allele/Variant
Source: rs779367922
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319174C>T

(GRCh38)13:32319103T>C

(Homo sapiens)
Allele/Variant
Source: rs397508057
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319103T>C

(GRCh38)13:32319181G>C

(Homo sapiens)
Allele/Variant
Source: rs397507603
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319181G>C

(GRCh38)13:32316446A>C

(Homo sapiens)
Allele/Variant
Source: rs138705202
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316446A>C

(GRCh38)13:32316481G>T

(Homo sapiens)
Allele/Variant
Source: rs1593880678
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316481G>T

(GRCh38)13:32319327T>G

(Homo sapiens)
Allele/Variant
Source: rs81002805
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319327T>G

(GRCh38)13:32315355A>G

(Homo sapiens)
Allele/Variant
Source: rs551887850
Genes: BRCA2 (Hsa), ZAR1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315355A>G

(GRCh38)13:32315507C>G

(Homo sapiens)
Allele/Variant
Source: rs1026273725
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315507C>G

(GRCh38)13:32315669T>C

(Homo sapiens)
Allele/Variant
Source: rs1593879845
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315669T>C

(GRCh38)13:32315672G>T

(Homo sapiens)
Allele/Variant
Source: rs930825419
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315672G>T

(GRCh38)13:32319168A>G

(Homo sapiens)
Allele/Variant
Source: rs921513445
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319168A>G

(GRCh38)13:32319170A>C

(Homo sapiens)
Allele/Variant
Source: rs80358445
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319170A>C

(GRCh38)13:32316421G>A

(Homo sapiens)
Allele/Variant
Source: rs1060499566
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316421G>A

(GRCh38)13:32316443G>T

(Homo sapiens)
Allele/Variant
Source: rs1593880555
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316443G>T

(GRCh38)13:32316444G>C

(Homo sapiens)
Allele/Variant
Source: rs1273462315
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316444G>C

(GRCh38)13:32316449T>G

(Homo sapiens)
Allele/Variant
Source: rs276174795
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316449T>G

(GRCh38)13:32363541A>C

(Homo sapiens)
Allele/Variant
Source: NC_000013.11:g.32363541A>C
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32363541A>C

(GRCh38)13:32363547C>T

(Homo sapiens)
Allele/Variant
Source: rs1287378096
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32363547C>T

(GRCh38)13:32363548A>G

(Homo sapiens)
Allele/Variant
Source: rs550087774
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32363548A>G

(GRCh38)13:32370401G>T

(Homo sapiens)
Allele/Variant
Source: rs397507979
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32370401G>T

(GRCh38)13:32370399C>G

(Homo sapiens)
Allele/Variant
Source: rs587782093
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32370399C>G

(GRCh38)13:32370561T>C

(Homo sapiens)
Allele/Variant
Source: rs81002801
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32370561T>C

(GRCh38)13:32376978C>T

(Homo sapiens)
Allele/Variant
Source: rs3764792
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32376978C>T

(GRCh38)13:32371124A>G

(Homo sapiens)
Allele/Variant
Source: rs81002851
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32371124A>G

(GRCh38)13:32379315A>T

(Homo sapiens)
Allele/Variant
Source: rs1566252482
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32379315A>T

(GRCh38)13:32385103C>A

(Homo sapiens)
Allele/Variant
Source: rs11571789
Genes: BRCA2 (Hsa), IFIT1P1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32385103C>A

(GRCh38)13:32315300G>A

(Homo sapiens)
Allele/Variant
Source: rs36221751
Genes: BRCA2 (Hsa), ZAR1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315300G>A

(GRCh38)13:32315647A>T

(Homo sapiens)
Allele/Variant
Source: NC_000013.11:g.32315647A>T
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315647A>T

(GRCh38)13:32315671A>G

(Homo sapiens)
Allele/Variant
Source: rs1429193506
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32315671A>G

(GRCh38)13:32316416T>C

(Homo sapiens)
Allele/Variant
Source: rs759888980
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316416T>C

(GRCh38)13:32316418G>T

(Homo sapiens)
Allele/Variant
Source: rs765644109
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316418G>T

(GRCh38)13:32317793C>T

(Homo sapiens)
Allele/Variant
Source: rs11571580
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32317793C>T

(GRCh38)13:32316530A>G

(Homo sapiens)
Allele/Variant
Source: rs1593880835
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32316530A>G

(GRCh38)13:32318598T>C

(Homo sapiens)
Allele/Variant
Source: rs206122
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32318598T>C

(GRCh38)13:32319336C>G

(Homo sapiens)
Allele/Variant
Source: rs1259689724
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319336C>G

(GRCh38)13:32319059G>A

(Homo sapiens)
Allele/Variant
Source: rs1555280319
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319059G>A

(GRCh38)13:32317629T>C

(Homo sapiens)
Allele/Variant
Source: rs11571578
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32317629T>C

(GRCh38)13:32319339T>G

(Homo sapiens)
Allele/Variant
Source: rs2138706036
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319339T>G

(GRCh38)13:32322152C>T

(Homo sapiens)
Allele/Variant
Source: rs11571596
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32322152C>T

(GRCh38)13:32323405G>A

(Homo sapiens)
Allele/Variant
Source: rs180863416
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32323405G>A

(GRCh38)13:32318738G>A

(Homo sapiens)
Allele/Variant
Source: rs11571585
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32318738G>A

(GRCh38)13:32318748G>A

(Homo sapiens)
Allele/Variant
Source: rs11571586
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32318748G>A

(GRCh38)13:32319056T>G

(Homo sapiens)
Allele/Variant
Source: rs1263784177
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319056T>G

(GRCh38)13:32319060A>G

(Homo sapiens)
Allele/Variant
Source: rs1060504621
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32319060A>G

(GRCh38)13:32325140A>G

(Homo sapiens)
Allele/Variant
Source: rs786202707
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32325140A>G

(GRCh38)13:32325145A>G

(Homo sapiens)
Allele/Variant
Source: rs2137446674
Genes: BRCA2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)13:32325145A>G