48766272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98487949-C-T

http://identifiers.org/hco/12/GRCh38#48766278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98487955-C-A

48766278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98487955-C-T

48766310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98487987-G-A

48766310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98487987-G-T

http://identifiers.org/hco/12/GRCh38#48766320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98487997-C-A

48766398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488077-G-A

48766398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488077-G-T

48766411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488090-G-A

48766432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488112-G-A

48766432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488112-G-T

48766578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488242-G-C

48766578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488242-G-T

http://identifiers.org/hco/12/GRCh38#48766607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98488269-C-A

48766885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488524-C-G

48766885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488524-C-T

48767002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488613-A-G

48767076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488697-T-C

48767216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98488839-A-G

48767405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489041-G-A

48767405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489041-G-T

48767708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489360-G-T

48767763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489426-C-T

http://identifiers.org/hco/12/GRCh38#48767782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98489444-C-A

48767782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489444-C-T

48767805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489472-G-T

48767971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489653-A-G

48768068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489753-T-C

48768158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489836-T-C

48768158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98489836-T-G

48768380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490021-G-A

48768380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490021-G-T

48768383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490024-A-T

http://identifiers.org/hco/12/GRCh38#48768436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98490073-C-A

48768436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490073-C-G

48768436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490073-C-T

48768519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490156-T-C

http://identifiers.org/hco/12/GRCh38#48768534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98490171-C-A

48768534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490171-C-G

48768534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98490171-C-T

48768600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98490240-G-A

48768669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98490309-C-T

48768711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98490351-G-A

48768889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98490516-G-T

http://identifiers.org/hco/12/GRCh38#48769033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98490650-A-C

48769033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98490650-A-G

48769093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98490714-G-A

http://identifiers.org/hco/12/GRCh38#48769134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98490753-C-A

48769134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98490753-C-T

48770546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98491127-A-G

48770660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491258-C-T

48770675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491273-G-T

48770694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491287-C-T

http://identifiers.org/hco/12/GRCh38#48770709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98491308-C-A

48770709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491308-C-G

48770709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491308-C-T

48770712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491311-G-C

48770763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491339-T-C

48770860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98491436-G-C

http://identifiers.org/hco/12/GRCh38#48770981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98491557-C-A

48770981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491557-C-G

48770981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491557-C-T

48770988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491580-A-G

http://identifiers.org/hco/12/GRCh38#48771018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98491612-C-A

48771018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491612-C-T

48771020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491614-G-T

48771083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491660-A-T

48771166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491681-A-G

http://identifiers.org/hco/12/GRCh38#48771172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98491687-C-A

48771172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491687-C-T

http://identifiers.org/hco/12/GRCh38#48771188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98491696-C-A

http://identifiers.org/hco/12/GRCh38#48771251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98491735-C-A

48771326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491851-A-G

48771336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491861-C-T

48771358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491883-A-T

48771390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491915-T-C

http://identifiers.org/hco/12/GRCh38#48771455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98491972-A-C

48771455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98491972-A-T

48771531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98492055-T-C

48771553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98492087-G-A

48771553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98492087-G-T

48771568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98492102-C-T

http://identifiers.org/hco/12/GRCh38#48771675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98492180-C-A

48771675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98492180-C-G

48771675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98492180-C-T

48771725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98492227-G-A

48772034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 98492536-A-G

48772110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98492612-A-G

48772125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98492627-G-C

48772125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98492627-G-T

48772621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493109-G-A

48772621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493109-G-T

48772857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493333-T-C

48772965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493422-T-A

48772965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493422-T-G

48773247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493716-T-A

48773247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493716-T-C

48773248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493717-A-T

http://identifiers.org/hco/12/GRCh38#48773337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98493805-C-A

48773337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493805-C-G

48773337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493805-C-T

48773356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493826-G-A

48773356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493826-G-C

48773356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493826-G-T

48773400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493861-G-A

48773400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493861-G-T

48773429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98493883-G-T

48773516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98493968-T-C

48773657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494109-T-C

http://identifiers.org/hco/12/GRCh38#48773682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98494141-C-A

48773699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494157-T-G

48773712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494170-G-A

48773712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494170-G-C

http://identifiers.org/hco/12/GRCh38#48773760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98494216-C-A

48773760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494216-C-G

48773760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494216-C-T

48773813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494273-G-T

48773814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494274-G-C

48773828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494288-G-A

48773828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494288-G-T

http://identifiers.org/hco/12/GRCh38#48774066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98494524-A-C

http://identifiers.org/hco/12/GRCh38#48774148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98494591-C-A

48774291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494688-G-A

48774291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494688-G-T

48774293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98494695-G-A

http://identifiers.org/hco/12/GRCh38#48774426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98494799-C-A

48774426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98494799-C-T

48774455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98494828-C-G

48774455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98494828-C-T

48774542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98494915-G-A

48774745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98495099-G-A

48774751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98495105-G-C

48774751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 98495105-G-T

48774803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495157-A-G

48774833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495188-T-C

48775016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98495320-A-G

48775019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98495323-G-A

48775019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 98495323-G-T

48775249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495554-G-A

48775498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495802-T-C

48775555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495861-G-A

48775555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495861-G-C

48775555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495861-G-T

48775602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495897-G-A

48775602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495897-G-C

48775616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495911-C-G

48775616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98495911-C-T

48775665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98495971-T-A

http://identifiers.org/hco/12/GRCh38#48775712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98496018-C-A

48775805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98496084-C-T

48775902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98496177-G-A

48775902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98496177-G-C

http://identifiers.org/hco/12/GRCh38#48775955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98496230-C-A

48775955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98496230-C-T

http://identifiers.org/hco/12/GRCh38#48775960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98496235-C-A

48776055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98496330-T-G

48776099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98496373-G-A

48776099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98496373-G-C

48776183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98496462-G-A

48776200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98496494-G-A

48776201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98496495-G-A

48776201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98496495-G-T

http://identifiers.org/hco/12/GRCh38#48776254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98496548-C-A

48776254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98496548-C-T

48776263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 98496557-G-C

http://identifiers.org/hco/12/GRCh38#48776275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98496569-C-A

48776344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98496638-G-A

48776484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98496795-A-G

48776487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98496798-G-A

48776514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98496825-G-A

48776547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98496858-G-A

http://identifiers.org/hco/12/GRCh38#48776609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98496923-C-A

48776609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98496923-C-T

48776622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98496936-T-C

48776705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497420-G-A

48776705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497420-G-T

48776805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497512-G-C

http://identifiers.org/hco/12/GRCh38#48776934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98497610-C-A

48776979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497658-T-A

48777016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497697-G-T

48777028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497709-T-C

48777049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497728-G-T

48777055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497733-T-A

48777055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497733-T-C

48777059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98497737-G-A

48777151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98497828-A-G

http://identifiers.org/hco/12/GRCh38#48777169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98497846-C-A

48777169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98497846-C-T

48777184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98497861-A-G

48777288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98497958-T-C

48777319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98497989-A-G

48777319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98497989-A-T

48777323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98497993-G-A

48777560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498214-C-T

48777620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98498281-A-G

48777825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498482-T-C

48777827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498484-G-T

http://identifiers.org/hco/12/GRCh38#48777842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98498502-C-A

48777842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498502-C-T

http://identifiers.org/hco/12/GRCh38#48777878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98498560-C-A

http://identifiers.org/hco/12/GRCh38#48777882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98498564-C-A

48777882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498564-C-G

48777882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498564-C-T

48777885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498567-A-G

48777885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498567-A-T

48777921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498603-G-C

48777973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498658-C-T

48778001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498687-G-A

48778001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498687-G-C

48778001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498687-G-T

http://identifiers.org/hco/12/GRCh38#48778008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98498694-C-A

48778008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498694-C-T

48778052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498736-G-A

48778052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498736-G-T

48778056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498740-G-A

48778075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98498759-G-C

48778101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98498784-G-A

48778101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98498784-G-T

48778171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98498855-G-A

48778171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98498855-G-T

48778268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 98498954-T-C

48778287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 98498974-C-G

48778299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98498986-C-T

48778304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98498991-C-T

48778310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98498997-A-G

http://identifiers.org/hco/12/GRCh38#48778312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98498999-A-C

http://identifiers.org/hco/12/GRCh38#48778435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98499105-C-A

48778435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499105-C-T

48778438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499108-G-T

http://identifiers.org/hco/12/GRCh38#48778495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98499163-C-A

48778501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499169-G-A

48778501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499169-G-T

48778546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499213-G-A

48778546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499213-G-C

48778546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499213-G-T

http://identifiers.org/hco/12/GRCh38#48778549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98499216-C-A

http://identifiers.org/hco/12/GRCh38#48778550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98499217-C-A

48778555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499223-A-G

http://identifiers.org/hco/12/GRCh38#48778570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98499238-A-C

48778570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499238-A-G

48778769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499444-A-G

http://identifiers.org/hco/12/GRCh38#48778924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98499527-A-C

48778924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499527-A-T

48779020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499588-G-A

48779071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499624-G-A

48779113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499646-C-G

48779255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499751-A-G

48779399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98499868-C-G

http://identifiers.org/hco/12/GRCh38#48779570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98500073-C-A

http://identifiers.org/hco/12/GRCh38#48779587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98500090-C-A

48779614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98500117-C-T

48779657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98500161-G-C

48779743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98500242-G-A

48780227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98500676-T-A

48780522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98500915-C-G

48780607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98500997-A-G

48780752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98501153-A-G

48782288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98501566-G-A

48782408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98501666-C-T

48782441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98501676-A-G

http://identifiers.org/hco/12/GRCh38#48782563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98501747-C-A

48782563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98501747-C-T

48782725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98501909-G-A

48782772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98501956-T-C

48782871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98502055-G-A

48782932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98502116-G-T

http://identifiers.org/hco/12/GRCh38#48783159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98502340-C-A

48783183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98502364-C-T

http://identifiers.org/hco/12/GRCh38#48783545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98502695-C-A

48783545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98502695-C-T

48784926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98503975-T-C

48785583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98504349-C-T

http://identifiers.org/hco/12/GRCh38#48785950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98504668-A-C

http://identifiers.org/hco/12/GRCh38#48786145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98504851-A-C

48786250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98504957-G-T

48786321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505017-C-T

48786861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505219-G-C

http://identifiers.org/hco/12/GRCh38#48787276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98505667-A-C

48787277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505668-C-T

48787370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505763-G-C

http://identifiers.org/hco/12/GRCh38#48787411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98505802-C-A

48787411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505802-C-G

48787458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505839-T-C

48787502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505880-C-G

48787502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98505880-C-T

48788693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98506931-T-G

48788871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron variant
orthologous variants: 98507062-G-A

48788871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron variant
orthologous variants: 98507062-G-T

48788898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98507078-G-A

48788898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98507078-G-T

48788916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98507096-G-C

48788916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98507096-G-T

http://identifiers.org/hco/12/GRCh38#48788931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#98507118-C-A

48788931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98507118-C-G

48788931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98507118-C-T

48788932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98507119-T-A

48788932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98507119-T-C

48788932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98507119-T-G

http://identifiers.org/hco/12/GRCh38#48788938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#98507125-C-A

48788938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98507125-C-T

http://identifiers.org/hco/12/GRCh38#48789022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#98507218-C-A

48789022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98507218-C-T

48789041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98507235-T-C

48789440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98507633-G-A

48789697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 98507852-G-A

48789793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98507958-G-A