92085369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4105023-G-A

92085574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4105240-A-G

92085703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4105366-A-G

92085726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4105387-T-A

92085740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4105401-A-G

http://identifiers.org/hco/7/GRCh38#92086139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4105514-A-C

92086139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4105514-A-T

92086214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4105579-A-G

92086297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4105649-C-G

92086306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4105658-T-A

92086306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4105658-T-C

92086354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4105706-G-A

http://identifiers.org/hco/7/GRCh38#92086373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4105725-C-A

92086373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4105725-C-G

92086373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4105725-C-T

92086386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4105738-A-G

http://identifiers.org/hco/7/GRCh38#92086520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4105880-C-A

92086520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4105880-C-T

92087967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4106841-A-T

http://identifiers.org/hco/7/GRCh38#92088176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4107008-C-A

92088176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4107008-C-G

92088183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4107015-T-C

92088360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4107165-A-G

92088426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4107214-A-G

92088627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4107446-G-T

92088920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4107756-A-G

92088924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4107760-G-A

92089236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108280-A-T

92089240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108287-A-G

92089256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108303-A-G

92089370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108422-C-T

92089386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 4108437-G-A

92089386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 4108437-G-C

92089445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4108496-T-A

92089445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4108496-T-C

92089447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4108498-T-C

92089447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4108498-T-G

92089480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4108531-T-A

92089480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4108531-T-G

92089481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4108532-A-G

92089481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4108532-A-T

http://identifiers.org/hco/7/GRCh38#92089493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4108544-C-A

92089533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108584-T-C

92089539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108589-A-G

92089539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108589-A-T

92089736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108790-T-A

92089760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108814-T-A

92089829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108862-A-G

92089847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108876-T-A

92089847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108876-T-G

http://identifiers.org/hco/7/GRCh38#92089877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4108912-A-C

92089877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108912-A-G

92089908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108942-G-C

92089908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4108942-G-T

92092606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4110120-T-G

http://identifiers.org/hco/7/GRCh38#92092999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4110187-A-C

http://identifiers.org/hco/7/GRCh38#92093002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4110190-C-A

http://identifiers.org/hco/7/GRCh38#92093009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4110197-A-C

92093051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4110236-A-G

92093093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 4110278-G-A

92093099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 4110284-C-G

92093099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 4110284-C-T

92093150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4110329-G-T

92093182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4110361-G-A

92093450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4110594-T-A

92093508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4110649-A-G

http://identifiers.org/hco/7/GRCh38#92093590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4110739-A-C

http://identifiers.org/hco/7/GRCh38#92094963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4111083-C-A

92094963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4111083-C-T

92095065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4111180-T-C

92095080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4111195-T-G

92095133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4111248-A-G

92095142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4111257-G-A

92095142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4111257-G-C

92095142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4111257-G-T

http://identifiers.org/hco/7/GRCh38#92097303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4114685-A-C

92097303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4114685-A-G

92097303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4114685-A-T

92097320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4114702-G-A

92097320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4114702-G-T

92097336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4114718-T-A

92097336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4114718-T-C

92097416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4114979-T-C

http://identifiers.org/hco/7/GRCh38#92097419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4114982-A-C

http://identifiers.org/hco/7/GRCh38#92097420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4114983-A-C

92097456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115057-T-C

92097496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115099-A-T

92097516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115115-C-T

92097517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115116-C-T

92097533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115132-G-A

92097533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115132-G-T

http://identifiers.org/hco/7/GRCh38#92097549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4115148-A-C

92097549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115148-A-G

92097609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4115204-T-G

92097908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115615-G-A

http://identifiers.org/hco/7/GRCh38#92097936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4115641-C-A

http://identifiers.org/hco/7/GRCh38#92097964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4115665-C-A

92098076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115772-G-A

92098076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115772-G-C

92098076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115772-G-T

92098100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115796-T-C

92098140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4115836-T-A

92098140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4115836-T-G

http://identifiers.org/hco/7/GRCh38#92098228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4115923-A-C

92098228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4115923-A-G

92098356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4116028-T-C

92098447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4116109-A-G

92098527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4116184-G-A

92098561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4116217-T-G

92099043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117120-C-G

92099043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117120-C-T

92099068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117143-T-G

92099412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117430-A-G

92099488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117503-C-T

http://identifiers.org/hco/7/GRCh38#92099544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4117583-C-A

92099544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117583-C-G

92099546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117585-G-T

http://identifiers.org/hco/7/GRCh38#92099622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4117650-C-A

92099622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117650-C-T

http://identifiers.org/hco/7/GRCh38#92099623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4117651-A-C

92099623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117651-A-G

92099623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117651-A-T

92099634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117676-A-G

92099641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117686-A-G

92099813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4117866-A-G

92099813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4117866-A-T

92099953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4117986-T-A

92100020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118055-A-T

92100070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118085-T-C

92100084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118099-G-A

92100084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118099-G-T

92100105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118120-C-G

92100186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118201-T-C

92100711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118813-G-T

92100772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118940-G-A

92100773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4118941-C-T

92101008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4119159-C-T

http://identifiers.org/hco/7/GRCh38#92101126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4119248-C-A

92101154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4119276-G-A

92101154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4119276-G-C

92101161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4119283-G-A

92101161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4119283-G-T

92102353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120124-G-T

92102403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120169-T-C

92102439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120196-G-A

92102439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120196-G-T

92102493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120215-C-T

92102517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120221-A-G

92102544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120248-G-A

92102549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120253-A-G

92102551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120255-T-C

http://identifiers.org/hco/7/GRCh38#92102557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4120261-C-A

92102557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120261-C-G

92102608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120313-A-G

92102722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120427-G-A

92102722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120427-G-C

92102731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120436-G-A

92102731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120436-G-C

92102731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120436-G-T

http://identifiers.org/hco/7/GRCh38#92102750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4120455-C-A

92102758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120463-G-A

92102758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 4120463-G-C

92102784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120489-C-T

http://identifiers.org/hco/7/GRCh38#92102834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4120539-C-A

92102841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120546-G-A

92102841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120546-G-T

92103765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120782-A-G

92103855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120870-T-C

92103948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4120935-T-G

http://identifiers.org/hco/7/GRCh38#92103997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4120984-A-C

92104099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4121051-C-T

92104117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4121067-A-G

92104863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4121773-A-G

92104891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4121799-A-G

92104896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4121804-C-G

92104901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4121809-C-G

92104923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4121832-G-A

92105107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4122149-T-C

92105223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4122243-C-G

92105398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4122392-C-T

92105502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4122467-T-C

92105561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4122506-T-G

http://identifiers.org/hco/7/GRCh38#92105802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4122743-C-A

92105802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4122743-C-T

92106830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4126713-T-C

92106955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4126867-A-G

92106972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4126884-C-G

http://identifiers.org/hco/7/GRCh38#92107219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4127117-A-C

92107219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127117-A-G

92107219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127117-A-T

92107365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4127258-C-T

92107399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4127292-G-T

92107497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127376-G-A

92107497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127376-G-T

92107500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127379-T-A

http://identifiers.org/hco/7/GRCh38#92107513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4127391-C-A

92107513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127391-C-G

92108115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127488-A-G

92108199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127572-T-C

http://identifiers.org/hco/7/GRCh38#92108323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4127684-A-C

http://identifiers.org/hco/7/GRCh38#92108602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4127936-A-C

92108641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 4127975-G-A

92108641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 4127975-G-C

92108645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 4127978-T-G

http://identifiers.org/hco/7/GRCh38#92108710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4128036-C-A

http://identifiers.org/hco/7/GRCh38#92109027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4128298-C-A

92109027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4128298-C-G

92109027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4128298-C-T

92109031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4128302-G-A

92109031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4128302-G-C

92109031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4128302-G-T

92110108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4129643-T-C

92110250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4129780-A-G

92110499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4130031-C-T

92110739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4130270-A-T

92110875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4130366-A-T

92110906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4130393-A-G

92111106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4130561-A-G

92111745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4130851-G-A

92112887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132483-T-A

92112891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132487-G-C

92112891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132487-G-T

92112924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132521-T-C

92113039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132583-A-G

92113063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132609-A-T

92113157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132670-A-G

92113162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132675-T-G

http://identifiers.org/hco/7/GRCh38#92113176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4132689-C-A

92113181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132694-G-A

92113181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132694-G-T

92113283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132782-T-A

92113283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132782-T-G

92113310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132809-G-A

92113310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132809-G-T

92113335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132821-G-T

http://identifiers.org/hco/7/GRCh38#92113408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4132880-C-A

92113408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132880-C-T

http://identifiers.org/hco/7/GRCh38#92113447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4132925-C-A

92113468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4132936-T-C

92113557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4133027-A-G

http://identifiers.org/hco/7/GRCh38#92113605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4133072-C-A

92113872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4133333-A-G

http://identifiers.org/hco/7/GRCh38#92113891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4133353-C-A

92113893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4133355-T-C

92113908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4133370-G-T

92113989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4133439-T-A

http://identifiers.org/hco/7/GRCh38#92114306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4133695-C-A

92114312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4133697-G-A

92114476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4133836-G-C

92114510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4133866-T-G

http://identifiers.org/hco/7/GRCh38#92116917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4136211-A-C

92116921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4136215-G-T

http://identifiers.org/hco/7/GRCh38#92117005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4136415-C-A

92117030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4136442-T-C

92117030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4136442-T-G

92117131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4136547-C-T

92117186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4136602-T-C

92117215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4136631-A-G

92117253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4136666-A-G

92117295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4136692-A-G

92117403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4136708-T-A

92117403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4136708-T-C

92117403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4136708-T-G

http://identifiers.org/hco/7/GRCh38#92117443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4136748-C-A

http://identifiers.org/hco/7/GRCh38#92117527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4136806-C-A

92117527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4136806-C-T

92118638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4137897-G-A

92118638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4137897-G-T

92118675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4137954-T-A

92118675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4137954-T-C

http://identifiers.org/hco/7/GRCh38#92118764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4138028-C-A

http://identifiers.org/hco/7/GRCh38#92119122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4138345-C-A

92119124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4138347-A-T

92119442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4138647-G-A

92119525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4138712-G-A

92119773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4138957-T-C

92122863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4141641-A-G

92123150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: synonymous variant
orthologous variants: 4141875-T-C

92123448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142138-A-G

92123452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142142-T-A

92123452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142142-T-C

92123452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142142-T-G

92123718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142373-T-C

92123726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4142380-G-A

92123726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4142380-G-C

92123803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: missense variant
orthologous variants: 4142457-A-G

92123833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: missense variant
orthologous variants: 4142487-C-T

92123891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142540-G-T

92123906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142554-G-A

92123906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142554-G-T

92123963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142593-T-A

92123963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142593-T-C

92123995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142618-G-A

92123995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4142618-G-T

92126082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4149011-T-C

92126132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4149058-A-G

http://identifiers.org/hco/7/GRCh38#92126192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4149081-C-A

92126192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4149081-C-T

92126236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4149103-A-G

92126251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: splice donor variant
orthologous variants: 4149118-A-G

92126279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: synonymous variant
orthologous variants: 4149150-T-C

92126372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: missense variant
orthologous variants: 4149243-A-T

http://identifiers.org/hco/7/GRCh38#92126434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4149304-A-C

92126460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4149330-A-G

92127100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4149791-A-G

92127255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4149938-G-A

92127335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4150014-T-G

92127395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4150073-G-C

92127395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4150073-G-T

92127400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4150078-A-G

92127488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4150128-T-C

92127512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: synonymous variant
orthologous variants: 4150152-T-C

92127539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: synonymous variant
orthologous variants: 4150179-T-C

92127542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: synonymous variant
orthologous variants: 4150182-C-T

92127652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4150297-G-C

92127653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4150298-G-A

92128850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151147-G-A

92128850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151147-G-T

92128937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: synonymous variant
orthologous variants: 4151235-G-A

92128937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: stop gained
orthologous variants: 4151235-G-C

92129119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151394-T-G

92129121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151396-T-A

92129121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151396-T-G

92129162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151437-T-C

92129162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151437-T-G

92129173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151448-T-A

92129173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4151448-T-C

http://identifiers.org/hco/7/GRCh38#92129203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4151478-C-A

92131366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152571-G-A

92131486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152677-T-G

92131490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152681-T-C

92131652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152817-T-C

92131748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152902-T-C

http://identifiers.org/hco/7/GRCh38#92131751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4152905-C-A

92131751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152905-C-G

92131751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152905-C-T

92131752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152906-T-A

92131752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152906-T-C

92131752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152906-T-G

92131763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152917-G-A

92131763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4152917-G-T

92131780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 4152934-A-T

92131795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 4152949-A-G

92131804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 4152958-T-C

92131858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 4153012-G-A

92131858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 4153012-G-C

92131858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 4153012-G-T

92133588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, undefined
orthologous variants: 4153568-C-T

92133601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4153581-C-T

92133900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4153915-G-A

92134023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4154061-C-G

92134023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron variant
orthologous variants: 4154061-C-T

92134099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, undefined
orthologous variants: 4154084-A-G

92134099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, undefined
orthologous variants: 4154084-A-T

92134100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, undefined
orthologous variants: 4154085-G-A

92134149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, undefined
orthologous variants: 4154111-T-C

92134149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, undefined
orthologous variants: 4154111-T-G

http://identifiers.org/hco/7/GRCh38#92134160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4154122-A-C

92134239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 4154200-G-A

http://identifiers.org/hco/7/GRCh38#92134436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4154393-C-A

92134436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4154393-C-T

92134443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4154400-T-C

http://identifiers.org/hco/7/GRCh38#92134483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4154441-C-A

92134483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4154441-C-G

92134499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4154462-G-A

92134499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4154462-G-C

92134499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4154462-G-T

92134572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154519-T-C

92134572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154519-T-G

92134576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154523-T-C

92134618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154566-G-T

92134678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154622-T-C

92134686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154630-T-C

http://identifiers.org/hco/7/GRCh38#92134718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4154661-C-A

92134718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154661-C-T

http://identifiers.org/hco/7/GRCh38#92134733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4154677-C-A

92134733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154677-C-G

92134733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154677-C-T

92134742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154686-G-A

92134742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154686-G-T

92134747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154691-G-A

92134747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4154691-G-T