125443155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36792350-G-A

125443257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36792253-T-C

125443770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791904-G-A

125443770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791904-G-C

125443778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791896-A-G

125443904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791767-A-T

125444155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791442-C-G

125444208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791386-G-C

125444252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791334-G-A

125444640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36791193-G-A

125444882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790976-G-A

125444887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790971-C-T

125444919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790949-C-T

125444947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790911-T-C

125445140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790719-G-A

125445140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790719-G-C

125445418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790477-T-C

125445567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790377-T-C

125445671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790299-G-A

125445671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3 prime UTR variant
orthologous variants: 36790299-G-T

125445876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36790100-G-A

125445876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36790100-G-T

http://identifiers.org/hco/11/GRCh38#125445885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36790091-C-A

125446133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789845-G-A

125446371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789663-T-G

125446994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789351-G-A

125447279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789084-T-C

125447639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36788822-T-G

125448301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787852-C-T

125448407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787760-T-C

125448410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787758-G-C

125448410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787758-G-T

125448597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787557-G-T

125448614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787539-G-A

125448614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787539-G-T

125448626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787527-G-T

125448648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787507-A-G

125449517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36785959-A-T

125449726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36785762-G-A

125449817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36785702-T-C

http://identifiers.org/hco/11/GRCh38#125449819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36785700-A-C

125449855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36785667-A-G

http://identifiers.org/hco/11/GRCh38#125449897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36785602-C-A

125450004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36785475-T-C

125451095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36784295-G-A

125451171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36784218-T-A

125451362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36782793-C-T

125451458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36782686-A-G

125451459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36782685-A-G

125451460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36782684-G-A

125451460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36782684-G-T

http://identifiers.org/hco/11/GRCh38#125451539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36782604-C-A

125451539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36782604-C-T

http://identifiers.org/hco/11/GRCh38#125451639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36782510-C-A

125451656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36782493-A-G

http://identifiers.org/hco/11/GRCh38#125451659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36782490-C-A

125452108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36782122-T-C

125452189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36782020-G-A

125452189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36782020-G-T

125452289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36781882-G-A

125452289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36781882-G-C

125452289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36781882-G-T

125452322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36781863-A-G

125452463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781727-G-C

125452463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781727-G-T

125452464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781726-G-T

125452497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781711-G-A

125452497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781711-G-T

125452561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781643-C-G

http://identifiers.org/hco/11/GRCh38#125452612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36781584-C-A

125452621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781575-T-C

125452631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781565-T-G

125452662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781536-G-A

http://identifiers.org/hco/11/GRCh38#125452833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36781394-C-A

125452833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36781394-C-G

125452833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36781394-C-T

http://identifiers.org/hco/11/GRCh38#125452866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36781380-A-C

http://identifiers.org/hco/11/GRCh38#125452872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36781374-C-A

125452954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781336-G-A

125452954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781336-G-C

125453359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781199-A-G

125453434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36781148-G-T

http://identifiers.org/hco/11/GRCh38#125453515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36781056-C-A

http://identifiers.org/hco/11/GRCh38#125454010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36780341-C-A

125454010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36780341-C-T

125454014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36780337-A-G

http://identifiers.org/hco/11/GRCh38#125454061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36780291-C-A

125454227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36780125-C-G

125454227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36780125-C-T

http://identifiers.org/hco/11/GRCh38#125454267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36780086-C-A

125454267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36780086-C-T

125454350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36780019-A-G

125454399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779980-T-C

http://identifiers.org/hco/11/GRCh38#125454406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36779973-A-C

http://identifiers.org/hco/11/GRCh38#125454476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36779905-C-A

125454476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779905-C-T

125454503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779878-C-T

125454504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779877-A-G

125454505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779876-G-A

125454505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779876-G-T

http://identifiers.org/hco/11/GRCh38#125455410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36779652-A-C

125455410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779652-A-G

http://identifiers.org/hco/11/GRCh38#125455440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36779622-A-C

125455440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36779622-A-G

125455468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779582-A-G

125455586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779511-G-T

125455640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779455-G-T

http://identifiers.org/hco/11/GRCh38#125455649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36779447-C-A

125455664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779432-G-A

125455664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779432-G-C

125455664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779432-G-T

http://identifiers.org/hco/11/GRCh38#125455692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36779404-C-A

125455705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779389-T-G

125455748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36779346-T-C

125455927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36779169-C-T

125456059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36779037-C-T

125456205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36778918-T-C

http://identifiers.org/hco/11/GRCh38#125456248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36778885-C-A

125456248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36778885-C-G

125456248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36778885-C-T

125456293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36778841-G-A

125456293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36778841-G-T

125458245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36776708-C-T

125458393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36776587-G-A

125460203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36775416-A-G

125460384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36775259-G-A

125460384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36775259-G-C

125460384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36775259-G-T

http://identifiers.org/hco/11/GRCh38#125460410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36775231-C-A

125460410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36775231-C-T

125460468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36774987-C-G

125460471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36774984-G-A

125460471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36774984-G-T

http://identifiers.org/hco/11/GRCh38#125460653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36774804-A-C

125460653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36774804-A-G

125460676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774779-G-A

125460699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774770-G-A

125460699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774770-G-C

125460721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774748-T-C

125460962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774533-G-A

125461059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774432-A-G

125461200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774270-G-A

125461204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36774266-G-T

125462226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36773263-T-C

http://identifiers.org/hco/11/GRCh38#125462282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36773209-A-C

125462447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36773052-T-A

125462473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36773031-A-T

125462538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36773011-G-A

125462736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36772901-T-C

125463423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36772253-C-G

125463458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36772222-C-T

125463662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36772041-G-A

http://identifiers.org/hco/11/GRCh38#125463684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36772019-C-A

http://identifiers.org/hco/11/GRCh38#125463709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36771994-C-A

125463790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36771946-T-A

125463914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36771824-G-A

125463963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36771778-T-C

125464265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770896-A-G

125464456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770707-G-C

125464529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770634-T-C

125464662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770519-A-G

125464663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770518-T-A

125464737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770323-A-G

125464738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770322-A-G

125464838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770216-G-A

http://identifiers.org/hco/11/GRCh38#125464850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36770204-C-A

125464850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770204-C-T

125464996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770059-G-A

125464996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36770059-G-C

125465247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36769359-A-G

125465632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36769044-C-T

125465686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768990-A-G

125465708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768966-G-C

125465781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768902-G-A

125465781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768902-G-C

125465992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768724-G-T

125466010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768707-G-C

125479042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36763925-G-A

125479265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36763711-T-C

125479574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36763327-C-T

http://identifiers.org/hco/11/GRCh38#125479697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36763198-A-C

125479697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36763198-A-T

125479737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36763160-A-G

125479758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36763141-T-C

125479975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36762953-T-C

125479986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36762942-T-C

125481143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36761951-T-C

125481536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36761738-C-T

125481670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36761604-G-A

http://identifiers.org/hco/11/GRCh38#125481793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36761484-C-A

125481834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36761437-G-T

125481852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36761419-G-A

125483259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36760810-A-G

125483766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36760019-T-G

125486191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36759214-C-T

125486716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36758215-A-G

125487151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757796-G-T

125487209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757741-G-A

125487237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757708-G-A

125487237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757708-G-C

125487500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757458-A-G

125487864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757086-T-G

125487899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757049-A-G

125489030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36756259-T-C

125489030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36756259-T-G

125489081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36756154-C-G

125489083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36756152-A-G

125489125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36756113-T-A

125489384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36755390-A-T

http://identifiers.org/hco/11/GRCh38#125489387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36755387-C-A

125489387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36755387-C-G

125489387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36755387-C-T

125491496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36751783-C-T

125493557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36747338-G-A

125493557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36747338-G-T

125493654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36747259-A-G

125493905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36747031-C-T

125493906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36747030-A-G

http://identifiers.org/hco/11/GRCh38#125493913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36747023-A-C

http://identifiers.org/hco/11/GRCh38#125494332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36746037-C-A

125494338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36746031-T-G

125494456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36745913-C-T

125494576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36745692-G-A

125494588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36745680-G-C

125494771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36745507-A-T

125494822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36745458-G-C

http://identifiers.org/hco/11/GRCh38#125495124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36745157-C-A

125495308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744976-G-A

125495372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744918-G-A

125495414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744885-C-G

125495425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744874-G-C

125495468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744828-A-G

125495520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744773-G-A

125495520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744773-G-C

125495520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744773-G-T

http://identifiers.org/hco/11/GRCh38#125495678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36744621-C-A

125495678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36744621-C-T

125495873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744474-G-T

125495899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744459-G-T

125495937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744431-C-G

125495937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744431-C-T

125495962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744403-G-A

125495962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744403-G-C

125495962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744403-G-T

125496193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36744145-C-T

125496376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36743990-G-T

http://identifiers.org/hco/11/GRCh38#125496389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36743977-C-A

125496690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36743668-G-A

125496699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36743660-C-T

125496706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36743653-C-G

125496869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36743508-T-C

http://identifiers.org/hco/11/GRCh38#125497050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36743380-C-A

http://identifiers.org/hco/11/GRCh38#125497099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36743342-C-A

125497099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36743342-C-T

http://identifiers.org/hco/11/GRCh38#125497105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36743336-C-A

125497179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36743263-G-A

125497179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36743263-G-T

125504621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36741053-C-T

http://identifiers.org/hco/11/GRCh38#125505876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36739799-C-A

125505897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36739774-T-A

125506195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36739477-A-G

125506207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36739449-T-C

http://identifiers.org/hco/11/GRCh38#125506340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36739311-C-A

125506608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36739005-T-C

125507752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36738607-A-T

125508072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36738295-C-G

125508222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36738165-C-T

125512528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36734667-C-T

125517071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36733427-T-A

125517151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36733347-G-C

http://identifiers.org/hco/11/GRCh38#125517356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36733107-A-C

125517714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36732750-G-A

125517751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36732715-G-T

125517899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36732526-T-A

125517956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36732489-C-T

125517963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36732482-T-C

http://identifiers.org/hco/11/GRCh38#125518227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36732312-C-A

125518483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36732095-G-T

125518530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron variant
orthologous variants: 36732061-A-G

http://identifiers.org/hco/11/GRCh38#125568411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36713165-C-A

125568455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36713118-C-T

125568976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36709028-T-C

125569229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36708840-G-A

125569229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36708840-G-C

125569279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36708808-C-G

http://identifiers.org/hco/11/GRCh38#125569392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36708710-C-A

125569392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36708710-C-T

125569566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708515-A-G

http://identifiers.org/hco/11/GRCh38#125569585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36708495-C-A

125569585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708495-C-T

125569602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708477-T-C

125569618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708461-G-A

125569618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708461-G-T

125569632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708447-G-A

125569632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708447-G-T

http://identifiers.org/hco/11/GRCh38#125569640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36708439-C-A

125569640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708439-C-G

125569640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708439-C-T

125569711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708358-G-T

http://identifiers.org/hco/11/GRCh38#125569803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36708256-C-A

125569803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708256-C-T

125569856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708215-A-G

125569870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708201-G-A

125569870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708201-G-T

125569980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708091-G-A

125570026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708045-A-T

125570048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36708015-A-G

http://identifiers.org/hco/11/GRCh38#125570398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36707718-C-A

125570398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36707718-C-T

125570561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36707551-G-A

125570645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36707472-T-C

125570767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36707356-C-T

125571329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36706844-G-C

125571474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36705792-C-T

125571552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36705511-A-G

125572361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36704730-G-C

125572374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36704717-G-A

125572420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36704672-A-G

125572609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36704494-T-C

125572720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36704378-A-G

125574699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36702474-T-A

125574700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36702473-G-A

125574700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36702473-G-T

125575422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36701063-G-A

125575422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36701063-G-T

http://identifiers.org/hco/11/GRCh38#125575423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36701062-C-A

125575423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36701062-C-T

http://identifiers.org/hco/11/GRCh38#125576378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36699412-A-C

125576378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36699412-A-G

125577488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697858-T-G

125577525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 36697822-C-T

125577622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697724-T-C

http://identifiers.org/hco/11/GRCh38#125577667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36697678-C-A

http://identifiers.org/hco/11/GRCh38#125577839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
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/9/GRCm39#36697554-C-A

125577839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697554-C-T

125577903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697512-G-A

125577954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697454-T-C

125578329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697161-G-A

125578336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697154-G-A

125578339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36697152-G-T

http://identifiers.org/hco/11/GRCh38#125579060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
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/9/GRCm39#36696835-C-A

125579157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36696750-A-G

125579846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36696141-T-C

125580276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36695702-A-T

125580292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36695685-G-T

http://identifiers.org/hco/11/GRCh38#125580346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36695632-A-C

125580346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36695632-A-G

125580637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36694495-T-G

125580658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36694474-G-T

125580753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36694396-T-A

125581133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36694211-G-A

125581133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36694211-G-T

125581365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36693984-A-G

http://identifiers.org/hco/11/GRCh38#125581434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#36693908-A-C

125581434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36693908-A-G

125582446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36693613-T-C

125583487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36691589-G-A

125583496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36691581-A-T

125583636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36691448-T-C

http://identifiers.org/hco/11/GRCh38#125583639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
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/9/GRCm39#36691445-C-A

125583639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36691445-C-T

125583654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36691430-G-A

125583678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36691406-C-G

125583707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36691381-G-A

http://identifiers.org/hco/11/GRCh38#125583792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36691298-C-A

125583792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36691298-C-T

125583980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36691142-T-A

125583980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36691142-T-C

125584240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36690887-A-T

125584246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36690881-A-T

http://identifiers.org/hco/11/GRCh38#125584506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36690640-C-A

125584555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36690592-G-T

125584615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36690517-G-T

125584980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36690127-C-T

125589322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36683600-G-A

http://identifiers.org/hco/11/GRCh38#125589411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36682281-A-C

http://identifiers.org/hco/11/GRCh38#125591912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36679757-A-C

125591912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679757-A-G

125591912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679757-A-T

125591929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679738-A-G

http://identifiers.org/hco/11/GRCh38#125591942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#36679725-C-A

125591942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679725-C-T

125591989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679697-G-A

125591989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679697-G-T

125592079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679651-C-T

125592092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679638-G-C

125592357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679382-T-G

125592393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36679363-C-T

125592456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36679305-G-A

125592486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36679275-C-T

125592515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36679245-C-G

125592515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36679245-C-T