121184832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131455240-G-A

121184832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131455240-G-T

121184859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131455213-A-G

121184995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131455079-G-T

http://identifiers.org/hco/1/GRCh38#121185019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131455064-A-C

121185019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131455064-A-G

121185019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131455064-A-T

http://identifiers.org/hco/1/GRCh38#121185191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131454905-C-A

121185191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131454905-C-G

121185200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131454896-G-C

http://identifiers.org/hco/1/GRCh38#121185327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131454769-C-A

121185327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131454769-C-T

121185355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131454741-A-G

121185355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131454741-A-T

121185398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131454706-C-G

121185398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131454706-C-T

http://identifiers.org/hco/1/GRCh38#121185581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131454561-C-A

121185581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131454561-C-T

http://identifiers.org/hco/1/GRCh38#121185593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131454549-C-A

121185593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131454549-C-T

121185646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131454498-C-T

121185681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131454464-T-G

http://identifiers.org/hco/1/GRCh38#121185892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131454270-A-C

121186049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131454153-T-G

http://identifiers.org/hco/1/GRCh38#121186303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131453927-A-C

121186583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131453644-C-G

121187026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 131453177-C-G

121187026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 131453177-C-T

121187439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5 prime UTR variant
orthologous variants: 131452748-A-T

121187551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131452636-G-A

121187821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131452386-G-T

121188238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131451962-T-G

121188255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131451945-G-A

121188333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131451867-G-A

121188582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131451614-G-C

121188967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131451216-T-G

121189171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131451030-T-C

121189267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131450926-G-T

121189421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131450772-A-T

121189653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131450521-A-G

121189814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131450382-G-A

121190270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131449799-G-C

121190695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131449415-G-A

121190732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131449378-T-A

121190986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131448987-G-A

121191628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131448684-G-T

121191673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131448641-G-A

121191898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131448462-T-C

121192145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131448073-G-A

121192170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131448048-C-T

121192528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131447755-G-T

121192736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131447565-C-T

121193065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131447275-C-T

http://identifiers.org/hco/1/GRCh38#121193280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131447093-A-C

121193441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446938-G-T

121193668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446493-T-C

121193668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446493-T-G

121193674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446487-T-C

121193675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446486-T-A

121193675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446486-T-G

121193688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446473-T-C

121193777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446395-C-T

121193813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446360-G-T

121193814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131446359-G-T

121195636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131445215-C-T

121196046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131444811-T-C

http://identifiers.org/hco/1/GRCh38#121196322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131444451-A-C

121196389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131444351-C-T

121196474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131444274-T-C

121197450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131443435-T-A

121197764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131443140-T-C

121197954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131442746-T-G

121198285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131442421-T-C

121198285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131442421-T-G

http://identifiers.org/hco/1/GRCh38#121198317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131442366-C-A

http://identifiers.org/hco/1/GRCh38#121198616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131442063-C-A

http://identifiers.org/hco/1/GRCh38#121198624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131442055-C-A

121198655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131442050-T-C

121198720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131441960-C-T

http://identifiers.org/hco/1/GRCh38#121198739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131441941-A-C

121198739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131441941-A-G

121199059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131441809-T-G

121199247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131441623-A-G

121199996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131441064-G-A

121200654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131440939-G-A

121200654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131440939-G-T

121200928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131440687-T-A

121201003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131440616-C-T

121201542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131439961-T-C

121201605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131439907-A-G

121201613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131439899-T-C

121202311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131439041-T-C

121202320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131439032-G-T

121203434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131438672-T-C

121203673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131438440-C-T

121203746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131438368-C-T

121205999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131434628-G-T

http://identifiers.org/hco/1/GRCh38#121206216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131434414-A-C

121206571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131434111-T-C

121206593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131434073-G-C

121206733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433975-G-A

121206733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433975-G-T

121206777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433935-G-C

121206777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433935-G-T

121207264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433510-G-A

121207379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433393-G-T

121207430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433352-C-G

http://identifiers.org/hco/1/GRCh38#121207438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131433344-C-A

121207667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433114-G-A

121207669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433112-A-G

121207755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131433026-G-T

121207830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131432938-G-C

121208068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131432721-C-T

121208295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131432473-G-A

121208295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131432473-G-C

121208295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131432473-G-T

121208420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131432351-T-A

121208787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131431984-G-A

http://identifiers.org/hco/1/GRCh38#121208969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131431867-C-A

121208969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131431867-C-G

121208969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131431867-C-T

121209151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131431438-A-G

121209283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131431293-G-C

121209334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131431242-A-G

121209581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131430783-G-T

121210227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131430133-G-C

http://identifiers.org/hco/1/GRCh38#121210295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131430060-C-A

121210295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131430060-C-G

121210447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131429914-C-G

http://identifiers.org/hco/1/GRCh38#121211092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131429193-A-C

121211232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131429040-A-G

121211294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131428921-G-A

121211511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131427841-T-A

121211561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131427795-G-T

121211635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131427735-A-G

121211644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131427726-T-C

121211976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131427251-A-G

121211990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131427203-A-T

http://identifiers.org/hco/1/GRCh38#121212112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131427081-C-A

121212445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131425001-A-T

121212483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131424963-G-A

121212483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131424963-G-T

121212526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131424923-C-T

http://identifiers.org/hco/1/GRCh38#121212571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131424868-C-A

121212571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131424868-C-G

121212589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131424850-A-G

121213652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131423992-G-A

121213674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131423970-A-G

121213834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131423821-T-C

http://identifiers.org/hco/1/GRCh38#121214562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131422619-A-C

121214562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131422619-A-T

121214590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131422597-G-T

121214941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131422279-A-G

121214961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131422258-A-G

121215714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131421563-C-G

121215714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131421563-C-T

121216451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131420745-T-C

121216512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131420683-A-T

121217018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131420149-G-A

121217410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131419748-T-C

121217705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131419450-A-G

121217705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131419450-A-T

121218043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131419156-A-G

121218113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131419086-T-C

121218122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131419075-T-A

121218122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131419075-T-C

121218458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131418755-G-A

121218458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131418755-G-C

121219029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131418361-C-T

121219965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131417626-A-G

121220164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131417423-G-A

121220164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131417423-G-T

121220301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131417288-T-A

121220319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131417270-A-G

http://identifiers.org/hco/1/GRCh38#121220552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131417035-C-A

121220776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131416818-G-A

121220776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131416818-G-C

http://identifiers.org/hco/1/GRCh38#121220785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131416807-A-C

121221235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131416358-C-T

121221855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131416074-G-A

121221874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131416055-G-T

121222126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131415293-G-A

121222126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131415293-G-T

121222193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131415235-C-T

121222515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131415118-G-A

121222963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131414802-C-T

121223410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131412083-A-T

121223563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131411944-G-C

121223801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131411736-T-A

121223801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131411736-T-C

http://identifiers.org/hco/1/GRCh38#121223908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131411636-C-A

121223908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131411636-C-T

121223960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131411576-A-G

http://identifiers.org/hco/1/GRCh38#121224085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131411455-A-C

121224107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131411432-G-A

121224301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131411046-A-G

121224358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131410984-G-T

121224438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131410673-T-A

121224438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131410673-T-G

121224702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131410417-G-T

121225386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409807-G-A

121225386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409807-G-T

121225405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409784-G-T

121225406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409783-G-A

121225406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409783-G-T

121225408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409781-G-A

121225408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409781-G-T

121225474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409706-A-G

121225611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409591-T-C

121226035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409467-T-A

121226035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409467-T-C

121226110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409398-C-T

121226239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131409285-T-G

121226843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131408711-T-C

121226910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131408644-G-A

121226910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131408644-G-T

121227344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131407386-C-G

121227392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131407349-A-T

121227427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131407301-T-C

121227442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131407284-C-G

121227524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131407241-G-A

121227694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131407128-C-G

121227694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131407128-C-T

121227864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406967-A-G

121227864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406967-A-T

http://identifiers.org/hco/1/GRCh38#121227932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131406906-C-A

121227965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406873-C-G

121227965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406873-C-T

121228008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406830-G-C

121228008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406830-G-T

121228025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406813-C-G

121228196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406643-G-C

121228487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406380-C-T

http://identifiers.org/hco/1/GRCh38#121228669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131406197-C-A

121228673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406193-T-C

121228677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406189-T-A

121228684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406186-C-T

http://identifiers.org/hco/1/GRCh38#121228794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131406091-C-A

121228794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131406091-C-G

121229205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131405662-G-A

121229205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131405662-G-T

121229241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131405629-A-G

http://identifiers.org/hco/1/GRCh38#121229356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131405517-C-A

121229356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131405517-C-T

121229405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131404078-G-T

121229443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131404040-A-T

121229522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131403966-T-A

121229746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131403753-G-A

121229869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131403630-T-C

121230362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131403144-C-G

121230362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131403144-C-T

121230441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402853-T-C

121230461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402838-T-A

121230466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402833-T-A

121230466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402833-T-C

121230466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402833-T-G

121230506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402793-T-C

121231273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402350-T-C

121231273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402350-T-G

121231373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402252-C-G

http://identifiers.org/hco/1/GRCh38#121231486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131402159-A-C

121231496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402149-G-A

121231651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131402003-A-T

121231770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131401897-G-A

121231770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131401897-G-T

http://identifiers.org/hco/1/GRCh38#121231835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131401834-C-A

121231956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131401713-C-T

121232011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131401658-G-A

121232250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131401423-G-T

121232502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131401166-C-T

http://identifiers.org/hco/1/GRCh38#121232647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131401029-A-C

http://identifiers.org/hco/1/GRCh38#121232904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131400865-C-A

121232904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131400865-C-T

121232958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131400825-A-G

121233502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131400483-C-G

121233566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131400421-C-T

121234129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131399799-C-G

121234129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131399799-C-T

121234310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131399618-T-C

121235323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131398431-G-A

121235343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131398411-G-A

121235547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131398251-C-T

121235607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131398184-A-G

121235607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131398184-A-T

121235812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131396943-A-G

121235931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131396780-G-A

121235933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131396778-A-T

http://identifiers.org/hco/1/GRCh38#121236599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131395980-A-C

121236599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131395980-A-G

121236662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131395940-C-T

121236704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131395899-G-A

121236704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131395899-G-T

121237171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131395452-T-C

121237405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131395246-C-T

121237682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131394978-C-T

http://identifiers.org/hco/1/GRCh38#121237816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131394841-C-A

http://identifiers.org/hco/1/GRCh38#121237919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131394755-C-A

121237919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131394755-C-T

121238567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131394283-T-C

http://identifiers.org/hco/1/GRCh38#121239308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131394070-C-A

121239308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131394070-C-G

121239380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131394003-T-A

121239393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131393990-A-G

121239480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131393930-T-C

121239584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131393833-G-T

http://identifiers.org/hco/1/GRCh38#121239597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131393821-C-A

http://identifiers.org/hco/1/GRCh38#121239690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131393733-A-C

121239788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131393594-G-T

121239862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131393520-C-G

121240283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131392812-T-G

121240397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131392713-A-G

121240489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131392623-G-C

http://identifiers.org/hco/1/GRCh38#121240500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131392613-A-C

121241366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131391922-T-C

121241457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131391792-T-C

121242077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131391195-G-A

121242360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131390895-G-T

121242701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131390555-A-G

121243672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131389570-T-C

121243775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131389291-T-A

121243775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131389291-T-C

121243789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131389282-T-G

121243790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131389281-T-G

121243818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131389260-T-A

121243818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131389260-T-G

121244452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131388616-G-A

121244789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131388360-C-T

http://identifiers.org/hco/1/GRCh38#121245580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131387073-C-A

121245673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131386981-A-G

121246217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131386571-T-G

121246411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131386376-G-A

121246468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131386319-T-C

121246537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131386250-T-C

121246634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131386156-A-G

121247036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131385782-A-G

121252212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131384415-T-G

121253360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131383467-T-A

121253446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131383371-G-C

121253697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131383151-C-T

http://identifiers.org/hco/1/GRCh38#121253824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131383032-C-A

121253902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131382944-A-G

121254540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131382087-C-T

121254657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131381992-C-T

http://identifiers.org/hco/1/GRCh38#121254677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131381974-A-C

121254880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131381825-G-C

121254880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131381825-G-T

121255063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131381636-G-C

121258079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131380910-T-C

121258138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131380850-C-T

121258209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131380791-G-A

121258230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131380769-C-G

121258326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131380684-C-T

121258368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131380645-C-T

121258875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131380413-A-G

121259023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131379603-T-C

http://identifiers.org/hco/1/GRCh38#121259113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131379514-C-A

121259113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131379514-C-T

http://identifiers.org/hco/1/GRCh38#121260199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131379140-C-A

121260199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131379140-C-G

121260334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131379026-G-A

121260358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131379002-T-C

121260359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131379001-G-T

121260391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131378968-C-T

121260426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131378933-G-A

121260669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131378682-G-A

121260748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131378629-T-G

121261264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131378436-A-G

121261378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131378332-T-C

121261711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131377992-A-G

121262145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131377163-T-C

121262181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131376759-G-A

http://identifiers.org/hco/1/GRCh38#121262202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131376738-C-A

121262453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131376143-C-T

121262634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131375964-G-A

121262872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131375547-G-A

http://identifiers.org/hco/1/GRCh38#121262874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131375545-A-C

121263078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131375392-G-T

121263503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131374952-T-A

121263643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131374810-C-T

121264019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131374510-T-C

http://identifiers.org/hco/1/GRCh38#121264432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131374128-C-A

121264507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131374061-C-T

121264553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131374014-G-A

121264553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131374014-G-C

121264553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131374014-G-T

121264706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131373854-C-T

121264880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131373714-T-A

121266999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131373310-T-C

http://identifiers.org/hco/1/GRCh38#121267048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131373260-C-A

121267140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131373175-T-C

121267490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131373123-C-T

121267512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131373101-A-G

http://identifiers.org/hco/1/GRCh38#121267577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131373051-A-C

121267933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131372612-A-T

121267957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131372490-T-C

121268122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131372295-A-G

121268191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131372226-C-T

121268256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131372150-A-T

121268346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131372049-T-C

121268423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371959-C-G

121268423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371959-C-T

http://identifiers.org/hco/1/GRCh38#121268431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131371951-C-A

121268431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371951-C-T

121268442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371942-C-T

121268444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371940-A-T

121268470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371914-G-C

121268667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371724-G-A

121268782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371613-C-T

121268874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371530-G-A

121278401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371296-A-T

121278477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371219-A-G

121278656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131371036-G-A

121278755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131370940-G-C

121278891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131370805-A-G

http://identifiers.org/hco/1/GRCh38#121279297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131370397-A-C

121279488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131370219-T-C

121279512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131370195-T-C

121279579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131370147-C-T

121279687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131370035-G-A

121280347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131369161-G-A

121280347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131369161-G-T

121280727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131368802-G-T

121280838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131368716-T-A

121281135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131368451-T-C

121281237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131368393-G-A

121281885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131367977-G-C

121282256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131367127-A-G

121282485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131366913-A-G

121282981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131366746-G-C

121283096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131366591-C-T

121283188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131366497-A-G

121283448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131366213-C-T

121283810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131365932-G-T

121283996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131365750-G-C

121284074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131365545-A-T

121284078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131365541-C-G

121284447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131364957-G-A

121284752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131364652-T-G

http://identifiers.org/hco/1/GRCh38#121284766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131364639-C-A

121284785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131364620-C-G

121285029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131364377-T-C

121290426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131363654-T-C

121292817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131360904-G-A

121292920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131360779-T-A

121292920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131360779-T-C

121292935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131360764-C-G

121293215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131360517-T-C

121293368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131360375-A-G

121293592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131359955-G-A

121293965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131359594-A-G

121293972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131359587-C-T

121294038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131359520-G-A

121294064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131359487-C-T

121294167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131359389-G-A

121294707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131358882-A-T

121294828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131358775-A-G

121296662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131358282-G-A

121296697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131358256-T-G

121296779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131358171-G-A

121296779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131358171-G-C

121296779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131358171-G-T

121296977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131357973-C-T

121297021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131357929-C-T

121297108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131357836-C-T

121297339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131357052-G-A

http://identifiers.org/hco/1/GRCh38#121297383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131356991-C-A

http://identifiers.org/hco/1/GRCh38#121297438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131356935-C-A

121297438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356935-C-T

121297462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356911-T-A

121297462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356911-T-C

121298463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356632-T-C

121298996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356153-T-A

121298996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356153-T-G

121299033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356103-G-A

121299033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131356103-G-T

121299410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131355722-G-T

121299432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131355701-C-T

121299817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131355321-A-T

121299818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131355320-G-A

121299818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131355320-G-T

121299998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131355146-G-A

121301214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131354496-G-A

121301331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131354405-G-A

121301745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131354310-T-G

121301773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131354282-G-A

121301958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131354112-G-T

121301966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131354104-T-A

121301972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131354098-G-T

121302006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131354024-G-A

121302158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131353888-G-A

121302158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131353888-G-C

121302167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131353879-C-T

121302191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131353859-A-T

http://identifiers.org/hco/1/GRCh38#121302205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131353845-A-C

121302358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353707-G-A

121302457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353611-C-T

121302612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353461-C-G

121302612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353461-C-T

121302632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353444-A-G

121302632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353444-A-T

121302734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353363-T-C

121302891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131353007-A-G

121303054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352855-G-A

121303290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352665-A-G

121303304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352651-T-C

121303519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352451-C-G

121303560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352410-G-A

121303560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352410-G-T

121303617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352350-T-C

121303650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352318-A-G

121303650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131352318-A-T

121305122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131351145-C-T

121305140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131351122-C-T

121305317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350961-C-T

http://identifiers.org/hco/1/GRCh38#121305335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131350953-C-A

121305386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350945-C-T

121305387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350944-G-A

121305547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350798-C-T

http://identifiers.org/hco/1/GRCh38#121305727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131350622-A-C

121305727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350622-A-G

121305961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350403-A-G

121305961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350403-A-T

121305967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350396-A-T

121305978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131350387-T-C

http://identifiers.org/hco/1/GRCh38#121306519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131349862-C-A

121307197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131349288-T-A

121307309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131349216-T-C

121307647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131348921-G-T

121307655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131348913-A-G

121307712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131348864-C-T

121307884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131348695-C-T

http://identifiers.org/hco/1/GRCh38#121315437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131347666-C-A

121315437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347666-C-T

121315487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347609-T-G

http://identifiers.org/hco/1/GRCh38#121315557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131347541-C-A

121315557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347541-C-T

121316129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347285-G-A

121316135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347279-G-A

http://identifiers.org/hco/1/GRCh38#121316154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131347260-C-A

121316154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347260-C-G

121316217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347229-T-C

121316443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131347002-A-T

121316509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131346954-T-C

121316589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131346872-A-G

121317982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131346002-C-T

121318043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131345941-G-A

121318534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131345422-T-C

121318611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131345349-C-T

121318679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131345287-G-A

121318679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131345287-G-T

121318860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131345121-A-G

121319144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344844-C-T

121319245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344747-C-G

http://identifiers.org/hco/1/GRCh38#121319262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131344736-C-A

121319262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344736-C-T

121319307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344702-G-A

121319339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344670-C-T

121319346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344663-G-A

121319815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344166-T-C

121319933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131344043-T-G

121320073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343903-A-G

http://identifiers.org/hco/1/GRCh38#121320074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131343902-C-A

121320074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343902-C-T

http://identifiers.org/hco/1/GRCh38#121320154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131343831-C-A

121320165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343820-G-A

121320183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343802-G-T

121320335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343662-T-C

121320363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343636-G-A

121320387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343612-C-T

121320520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343331-A-G

121320724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131343030-G-T

121320897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131342859-G-C

121323055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131341541-A-G

121323785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131341158-G-A

121323792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131341151-G-A

http://identifiers.org/hco/1/GRCh38#121323857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131341086-C-A

http://identifiers.org/hco/1/GRCh38#121324336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131339838-C-A

121324336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339838-C-T

121324413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339760-T-C

121324415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339758-G-A

121324563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 131339613-C-T

121324898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339386-C-T

121324965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339320-T-C

121325064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339239-T-C

121325112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339194-A-G

121325184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339124-C-T

http://identifiers.org/hco/1/GRCh38#121325212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131339097-C-A

http://identifiers.org/hco/1/GRCh38#121325213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131339096-A-C

121325218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131339091-T-C

http://identifiers.org/hco/1/GRCh38#121325373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131338945-C-A

121325373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131338945-C-G

121325502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131338827-G-T

121325738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131338183-G-T

121325965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131337969-C-T

121326042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131337892-A-G

121326602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131337001-G-T

http://identifiers.org/hco/1/GRCh38#121326703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131336906-C-A

121326870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131336750-T-C

121326928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131336703-G-A

121326932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131336699-A-G

121327943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131336454-C-T

http://identifiers.org/hco/1/GRCh38#121328061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131336373-C-A

121328302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131336137-A-G

121328447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131336055-T-G

121328516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335981-C-T

121329292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335863-A-G

121329297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335858-T-C

121329306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335850-A-G

121329506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335703-G-C

121329703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335518-G-A

121329744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335477-G-A

121329951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131335273-G-A

121330410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131334746-C-G

121330455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131334701-A-G

121330641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131334526-T-A

121330641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131334526-T-G

http://identifiers.org/hco/1/GRCh38#121330924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131333939-C-A

http://identifiers.org/hco/1/GRCh38#121333008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131331865-A-C

121333089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131331780-A-G

121334339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131330742-T-C

121334383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131330686-A-G

121336110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131330451-A-G

121336961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131329547-G-A

http://identifiers.org/hco/1/GRCh38#121337129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131329401-A-C

121338082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131328775-T-G

121338366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, undefined
orthologous variants: 131328502-G-C

121338521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131328296-G-T

121338523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131328294-T-G

121338526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131328291-T-C

121338566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131328209-T-C

121338606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131328173-C-T

http://identifiers.org/hco/1/GRCh38#121338614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131328165-A-C

121338614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131328165-A-G

121338636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131328143-A-G

121339044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131327685-A-G

121339848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131327208-T-C

121339904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131327152-T-C

121340086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131326980-A-G

121340534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131326482-G-T

121340919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131326116-T-A

121340919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131326116-T-C

121340919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131326116-T-G

121341064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131325973-T-A

http://identifiers.org/hco/1/GRCh38#121341080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131325958-C-A

http://identifiers.org/hco/1/GRCh38#121341389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131325594-A-C

121341405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131325578-A-G

121341447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131325500-G-A

121341460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131325484-A-T

http://identifiers.org/hco/1/GRCh38#121341850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131325195-C-A

121342317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324717-T-G

121342742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324388-T-C

121342825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324313-G-T

121342829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324309-G-A

121342829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324309-G-T

121342841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324297-C-T

121342910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324229-A-G

121343071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131324078-A-G

121343313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131323868-A-G

121346409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131322055-G-C

121346509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131321962-T-C

121347175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131321339-A-G

121347380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131321148-A-T

121349670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131316914-G-T

121350019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131316617-T-C

121350285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131316133-A-T

121350913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131315713-G-A

121351061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131315588-T-C

121351061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131315588-T-G

121351119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131315532-G-A

121351970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131314939-A-T

121352319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131314645-G-T

121352498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131314444-G-A

http://identifiers.org/hco/1/GRCh38#121355796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131312755-A-C

121355816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131312736-T-C

121356219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131312405-C-T

121356496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131312158-C-T

121356664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131312008-C-G

121356664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131312008-C-T

121356665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131312007-T-C

121358372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131309638-G-C

121358372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131309638-G-T

121358625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron variant
orthologous variants: 131309415-T-C

http://identifiers.org/hco/1/GRCh38#121360502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131308388-C-A

121360581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131308292-G-A

121360581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131308292-G-T

121360611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131308261-A-T

121360733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131308140-T-A

121360733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131308140-T-C

121361113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307764-G-T

121361471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307238-T-A

121361471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307238-T-C

121361570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307134-T-C

121361631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307074-A-G

121361635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307070-C-T

121361921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131306787-C-T

121362035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131306673-G-A

121362071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131306638-T-C

http://identifiers.org/hco/1/GRCh38#121362093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131306616-C-A

121362158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131306551-G-A

121362213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131306497-G-T

121362243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131306467-T-G

121362326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131306379-C-T

121362419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131306293-G-T

121362667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131306038-G-A

121362667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131306038-G-T

http://identifiers.org/hco/1/GRCh38#121362669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131306036-C-A

121362669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131306036-C-T

121362913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131296820-C-T

121364858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131292229-T-C

http://identifiers.org/hco/1/GRCh38#121365311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131291782-C-A

121365904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131291243-C-T

121365996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131291163-G-A

121366022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131291150-T-C

http://identifiers.org/hco/1/GRCh38#121367056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131289938-C-A

121367476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131289587-C-T

121367983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131289106-G-A

121367983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131289106-G-T

121368050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131289057-T-G

121368126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131289006-G-A

121368126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131289006-G-T

121368192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131288973-A-G

121368269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131288922-G-A

121368662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131288704-A-G

121368716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131288652-A-G

121368855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131288222-C-G

121368855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131288222-C-T

121369003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131288072-T-C

121369100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131287977-T-C

121369505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131287551-A-G

121369532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131287526-C-T

121369751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131287310-A-G

121371640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286748-C-T

121371706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286694-T-C

121371770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286659-T-A

http://identifiers.org/hco/1/GRCh38#121371979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131286485-A-C

121372141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286349-C-T

121372294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286240-G-A

121372294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286240-G-T

121372370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286183-C-T

121372437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131286146-C-T

121372597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131285979-G-A

http://identifiers.org/hco/1/GRCh38#121372713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131285865-C-A

121372987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131285578-C-T

121373291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131285119-T-C

121373341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131285064-A-G

121373674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131284897-A-G

121373706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131284867-A-T

121373934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131284668-T-A

121373934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131284668-T-C

121373934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131284668-T-G

121373945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131284657-G-C

121373945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131284657-G-T

121374040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131284572-A-G

121374622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283746-T-C

121374661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283674-G-A

121374801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283400-A-G

121374803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283398-G-C

121374809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283392-T-A

121374809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283392-T-C

121374913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131283288-G-A

http://identifiers.org/hco/1/GRCh38#121374937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131283264-C-A

121374937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 131283264-C-T

121374977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283219-C-G

121374977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283219-C-T

121375014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283182-A-T

121375041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131283155-A-G

121375058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283138-A-T

121375103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283097-A-G

121375110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283090-T-A

121375129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283075-A-G

121375690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282874-A-G

121375749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282813-G-A

121375890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282678-A-T

http://identifiers.org/hco/1/GRCh38#121375906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131282662-C-A

121375934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282638-G-A

121375940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282624-C-G

121375983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282582-C-G

121375983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282582-C-T

http://identifiers.org/hco/1/GRCh38#121375990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131282575-C-A

http://identifiers.org/hco/1/GRCh38#121376151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131282459-C-A

http://identifiers.org/hco/1/GRCh38#121376436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131282177-A-C

121376596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131282055-T-A

121376730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281922-A-G

121376944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281724-G-A

121376959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281709-T-A

121376959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281709-T-C

121376959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281709-T-G

http://identifiers.org/hco/1/GRCh38#121379060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131281513-A-C

121379284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281287-G-A

121379295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281276-C-T

121379316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281256-C-T

121379495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281124-C-T

121379538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131281090-C-T

121379670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131280980-A-T

http://identifiers.org/hco/1/GRCh38#121380168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131280544-C-A

121380351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131280357-G-A

121380351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131280357-G-T

121380353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131280355-C-T

121380359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131280349-A-G

121380382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131280322-C-T

121380430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131280282-C-T

121380721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131279992-G-T

121380809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131279911-G-A

http://identifiers.org/hco/1/GRCh38#121381551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131279187-C-A

121381681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131279056-C-G

121381740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131278997-T-C

121382367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131277736-C-T

121382436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131277669-C-T

http://identifiers.org/hco/1/GRCh38#121382489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131277617-C-A

121382508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131277598-G-A

http://identifiers.org/hco/1/GRCh38#121382944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131277165-A-C

121382944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131277165-A-G

http://identifiers.org/hco/1/GRCh38#121384305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131275739-C-A

121384407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131275638-C-T

121384955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131275090-T-A

121385554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131274577-T-C

121385589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131274540-G-A

121385589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131274540-G-T

121385817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131274318-T-C

http://identifiers.org/hco/1/GRCh38#121385838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131274297-C-A

121386095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131274051-C-G

121386095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131274051-C-T

121387405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131272535-A-G

121387525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131272417-C-G

121387525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131272417-C-T

http://identifiers.org/hco/1/GRCh38#121387598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131272317-A-C

121387623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131272293-T-A

121387712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131272204-T-C

121388060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271862-C-T

121388472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271397-T-A

121388588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271186-T-A

121390487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30584
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131268987-T-C