7686899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107371917-A-G

7688512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107379104-G-T

7688524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379116-G-T

7688611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379187-C-G

7688617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379193-G-A

7688617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379193-G-T

7688901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379599-C-T

7688990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379679-G-C

7689043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379729-T-A

http://identifiers.org/hco/11/GRCh38#7689094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107379780-C-A

7689189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107379834-G-A

7689308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380616-T-G

7689320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380628-C-G

7689320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380628-C-T

7689436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380743-G-A

7689444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380750-G-A

7689444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380750-G-C

7689487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380793-T-A

7689487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380793-T-C

7689492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380798-G-A

7689492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380798-G-C

7689492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380798-G-T

7689526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380831-G-A

7689526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380831-G-T

7689533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380838-A-G

7689533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107380838-A-T

http://identifiers.org/hco/11/GRCh38#7689620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107380904-C-A

7689620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380904-C-T

7689640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380920-A-G

7689640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380920-A-T

7689653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380930-C-G

7689653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107380930-C-T

http://identifiers.org/hco/11/GRCh38#7689740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107381012-C-A

7689740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381012-C-G

7689740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381012-C-T

7689753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381026-G-T

7689859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381125-C-G

7689933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107381186-T-C

http://identifiers.org/hco/11/GRCh38#7690014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107381258-C-A

7690014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107381258-C-G

7690014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107381258-C-T

7690066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381306-G-A

7690066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381306-G-T

7690083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381320-T-C

http://identifiers.org/hco/11/GRCh38#7690095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107381332-C-A

7690095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381332-C-G

http://identifiers.org/hco/11/GRCh38#7690109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107381346-C-A

7690109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381346-C-T

7690269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381511-C-T

7690278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381520-G-A

7690374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381605-C-G

7690374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381605-C-T

7690435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381770-T-C

7690452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381787-G-A

7690452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381787-G-C

7690536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381854-C-T

7690562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381881-C-T

7691074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383526-A-G

7691129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383573-G-A

7691129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383573-G-T

7691152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383596-T-C

7691179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383620-A-G

7691314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107383750-T-A

7691314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107383750-T-C

7691318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107383754-G-A

7691318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107383754-G-C

http://identifiers.org/hco/11/GRCh38#7691352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107383788-C-A

7691372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107383808-G-A

7691372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107383808-G-T

7691385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107383821-T-C

7691388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107383824-C-T

http://identifiers.org/hco/11/GRCh38#7691390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107383826-A-C

7691390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107383826-A-G

http://identifiers.org/hco/11/GRCh38#7691433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107383867-C-A

7691433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107383867-C-G

7691433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107383867-C-T

7691445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107383872-A-T

7691454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107383881-T-A

7691454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107383881-T-C

7691476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107383903-A-G

http://identifiers.org/hco/11/GRCh38#7691487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107383916-C-A

7691487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107383916-C-T

7691499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107383928-G-A

7691499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107383928-G-T

http://identifiers.org/hco/11/GRCh38#7691542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107383977-A-C

7691542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383977-A-G

7691651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384372-A-G

http://identifiers.org/hco/11/GRCh38#7691769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107384477-A-C

7691769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384477-A-G

7691789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384497-G-A

7691789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384497-G-T

7691801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384509-G-A

7691801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384509-G-T

7691894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107384601-A-G

7691921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107384628-T-C

http://identifiers.org/hco/11/GRCh38#7692060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107384747-C-A

7692060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107384747-C-G

7692060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107384747-C-T

7692076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107384763-G-T

http://identifiers.org/hco/11/GRCh38#7692079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107384766-C-A

7692079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107384766-C-T

7692276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107384950-G-A

7692342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107385013-T-C

7692427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107385092-T-G

7692677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385336-G-A

7692677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385336-G-T

7692733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107385362-A-T

7692835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385388-C-G

7692837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385390-T-A

7692962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385510-T-G

7692972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385520-C-T

7693012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385558-G-A

7693036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385583-T-C

7693051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107385601-G-A

http://identifiers.org/hco/11/GRCh38#7693749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107386265-C-A

7693944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107386468-G-A

7694218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387192-G-A

7694299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387277-C-G

7694299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387277-C-T

7694302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387280-C-T

7694428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387384-C-G

7694498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387450-A-T

7694559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387507-G-A

7694568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387515-G-A

7694698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387549-A-G

7694936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107387694-T-C

7694962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107387713-A-G

7695040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107387791-G-C

7695101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107387852-T-A

7695184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107387935-T-A

7695184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107387935-T-C

http://identifiers.org/hco/11/GRCh38#7695245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107387989-C-A

7695285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107388022-A-G

7695371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107388107-G-A

7695497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107388221-C-G

7695562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107388287-G-T

7695563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107388288-G-C

7695575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107388302-A-G

7695672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107388399-T-A

7695678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107388405-T-A

7695678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107388405-T-C

7695691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107388418-G-A

7695716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107388443-G-A

7695764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107388486-T-C

7695828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107388548-C-T

http://identifiers.org/hco/11/GRCh38#7695856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107388576-C-A

http://identifiers.org/hco/11/GRCh38#7696066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107388844-C-A

7696082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107388935-G-A

http://identifiers.org/hco/11/GRCh38#7696350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107389171-C-A

7696350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389171-C-G

7696350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389171-C-T

7696355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389176-G-A

7696355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389176-G-T

7696368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389189-G-A

7696368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389189-G-T

http://identifiers.org/hco/11/GRCh38#7696389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107389210-C-A

7696389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389210-C-T

7696407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389228-G-A

7696412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389233-C-T

7696439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389260-A-G

7696508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107389329-G-A

7696508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389329-G-C

7696522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389343-C-T

7696547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107389368-C-T

7696593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107389414-T-C

7696626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389447-C-T

7696672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389497-G-A

7696672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389497-G-C

7696726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107389547-T-C

7696783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389604-C-G

7696783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107389604-C-T

7696816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389637-G-A

7696816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389637-G-T

http://identifiers.org/hco/11/GRCh38#7696855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107389675-C-A

7696855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389675-C-T

http://identifiers.org/hco/11/GRCh38#7696870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107389690-C-A

7696870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389690-C-T

7696906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389725-A-T

7696911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389731-T-A

7696955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389790-T-A

7696955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107389790-T-C

7697004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389839-T-G

7697009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389844-T-G

7697040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107389903-T-A

http://identifiers.org/hco/11/GRCh38#7697080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107389939-A-C

7697322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107390140-G-A

7697754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107390427-G-C

7697754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107390427-G-T

7698631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391195-T-C

7698631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391195-T-G

7698644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391208-A-T

7698703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391277-G-T

7698724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391298-T-A

7698724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391298-T-C

7698917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391476-G-A

7698917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391476-G-T

7698927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391486-T-A

7698927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391486-T-C

7698939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391498-G-A

7698939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391498-G-C

7698939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107391498-G-T

7698947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107391506-G-A

7698947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107391506-G-T

7698991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391548-T-C

http://identifiers.org/hco/11/GRCh38#7699018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107391576-C-A

7699018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391576-C-G

7699039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391600-A-G

7699039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391600-A-T

7699177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391717-T-G

7699280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391804-G-A

7699280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391804-G-T

7699296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391823-C-G

7699296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391823-C-T

7699759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107391942-T-C

http://identifiers.org/hco/11/GRCh38#7699929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107392111-A-C

7699929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107392111-A-G

7699929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107392111-A-T

7699930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107392112-G-T

7700136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392301-T-C

7700136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392301-T-G

http://identifiers.org/hco/11/GRCh38#7700164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107392323-C-A

7700164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392323-C-T

7700187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392346-G-A

7700187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392346-G-T

7700200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392359-T-G

7700207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392366-A-G

7700207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392366-A-T

7700238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392386-G-A

7700238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107392386-G-T

7700357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107392502-G-A

7700357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107392502-G-C

7700357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107392502-G-T

7700690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107392826-C-G

http://identifiers.org/hco/11/GRCh38#7701320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107393157-C-A

7701320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393157-C-G

http://identifiers.org/hco/11/GRCh38#7701518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107393349-C-A

7701537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393366-G-A

7701538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393384-C-T

7701583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393437-A-G

7701658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393506-G-A

7701658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393506-G-T

http://identifiers.org/hco/11/GRCh38#7701667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107393515-C-A

7701667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393515-C-T

http://identifiers.org/hco/11/GRCh38#7701681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107393531-C-A

http://identifiers.org/hco/11/GRCh38#7701879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107393719-C-A

7701897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393737-C-G

7701897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393737-C-T

http://identifiers.org/hco/11/GRCh38#7702023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107393845-C-A

7702030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393852-G-A

7702030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393852-G-T

7702037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393859-C-T

7702038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393860-A-T

http://identifiers.org/hco/11/GRCh38#7702096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107393937-A-C

7702096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107393937-A-G

7702163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107393995-G-C

7702163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107393995-G-T

7702227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107394059-T-A

7702227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107394059-T-G

http://identifiers.org/hco/11/GRCh38#7702320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107394152-C-A

7702324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107394156-A-G

http://identifiers.org/hco/11/GRCh38#7702426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107394258-A-C

7702426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394258-A-G

7702442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394274-A-G

http://identifiers.org/hco/11/GRCh38#7702458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107394290-A-C

7702458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394290-A-G

7702458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394290-A-T

7702462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394294-T-A

7702462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394294-T-G

http://identifiers.org/hco/11/GRCh38#7702484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107394316-A-C

http://identifiers.org/hco/11/GRCh38#7702558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107394359-A-C

7702603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394406-C-T

7702680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394483-A-G

7702865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394799-G-A

7702952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107394888-G-C

7703084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395177-C-T

7703245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395338-T-C

7703272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395365-G-A

7703293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395386-G-A

7703367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395443-T-C

7703409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395492-A-T

http://identifiers.org/hco/11/GRCh38#7703549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107395615-C-A

7703549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395615-C-T

7703556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395622-G-A

7703556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395622-G-T

7703562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395628-T-A

7703562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395628-T-C

http://identifiers.org/hco/11/GRCh38#7703578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107395641-A-C

7703578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395641-A-G

7703769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107395798-C-T

7703822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395850-T-C

7703822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395850-T-G

7704244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107395956-T-C

7704383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107396335-A-G

7704398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107396350-C-T

7704610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107397262-G-A

7704610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107397262-G-C

7704610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107397262-G-T

7704701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107397351-T-C

7704706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107397356-A-G

7704729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107398744-A-G

http://identifiers.org/hco/11/GRCh38#7705048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107399036-A-C

7705229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107399198-G-T

7705270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107399238-G-T

7705398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107399384-G-T

http://identifiers.org/hco/11/GRCh38#7705412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107399398-C-A

7705430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107399417-T-A

7705430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107399417-T-G

7705471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107399457-A-G

7705626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107399609-G-T

7705656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 107399638-G-A

7705656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 107399638-G-T

7706082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107400044-T-G

7706093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107400055-T-C

7706145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107400097-T-C

7706244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107400194-T-G

http://identifiers.org/hco/11/GRCh38#7706307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#107400299-C-A

7706307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107400299-C-G

7706309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107400301-T-C

7706314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107400306-G-A

7706314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107400306-G-T

7706407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107400399-A-G

7706448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107400439-A-G