131134464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron variant
orthologous variants: 25173751-G-A

http://identifiers.org/hco/6/GRCh38#131134547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25173662-A-C

131135100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron variant
orthologous variants: 25173257-G-A

131135776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25172830-G-A

131135791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25172815-G-A

131135791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25172815-G-C

131135791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25172815-G-T

http://identifiers.org/hco/6/GRCh38#131135827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25172783-C-A

131135827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25172783-C-T

http://identifiers.org/hco/6/GRCh38#131135948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#25172680-C-A

131136002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25172627-G-A

131136167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25172468-T-C

131136167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25172468-T-G

131136309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25172322-T-A

131136309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25172322-T-C

http://identifiers.org/hco/6/GRCh38#131136393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25172243-C-A

131136629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25171937-G-A

131137687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25171553-T-C

131137913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25171343-T-C

131139248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25169086-T-C

131139593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25168384-C-T

131139710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25168295-G-A

131139788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25168224-G-C

131140175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25167927-C-T

131140237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25167863-G-T

131140368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25167765-A-G

http://identifiers.org/hco/6/GRCh38#131140482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25167659-A-C

131140543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25167598-A-G

131145213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25165698-T-C

131145285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 25165626-G-T

http://identifiers.org/hco/6/GRCh38#131145318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#25165593-C-A

131145318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 25165593-C-G

131145331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25165580-A-G

131145334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 25165577-G-A

131145335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25165576-T-C

131146539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164961-G-A

131148111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164646-T-C

131148151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164611-A-G

131148312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164435-G-T

131148451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164325-C-G

131148451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164325-C-T

131148470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164275-T-C

131148556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164196-G-A

131148563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25164189-T-A

http://identifiers.org/hco/6/GRCh38#131149728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25163124-A-C

131150161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25162577-G-T

131152095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25161557-C-G

131152315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25161339-T-C

131152335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25161319-A-G

131152393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25161262-T-G

131152462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25161194-C-T

131152508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25161154-T-C

131159787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25160224-C-T

131159900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25160116-T-A

131160068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25159928-A-G

131160068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25159928-A-T

131160069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25159927-A-T

131160157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 25159830-C-T

131160184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25159803-A-G

131160227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25159758-G-A

131160227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25159758-G-T

131160259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25159722-A-G

131160262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25159719-T-C

131160318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25159663-G-T

131160347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25159634-A-G

131160559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25159380-G-A

131161168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25158199-A-G

131161229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25158138-A-G

131161241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25158127-A-G

131162954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25156798-C-G

131162975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25156778-G-T

131163268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25156454-A-T

131163285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25156436-G-A

131163881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25148642-T-C

131164051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25148527-C-G

131164376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25148226-A-G

http://identifiers.org/hco/6/GRCh38#131164389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25148213-C-A

131164400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25148202-G-A

131164400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25148202-G-T

131164492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25148114-G-A

http://identifiers.org/hco/6/GRCh38#131164521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25148083-C-A

131164521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25148083-C-T

http://identifiers.org/hco/6/GRCh38#131164547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25148054-C-A

131164867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147735-A-G

131165242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147378-A-G

131165291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147330-A-G

131165322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147301-T-C

131165322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147301-T-G

131165327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147296-A-G

131165331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147292-T-C

131165333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147290-T-C

131165376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147246-T-C

131165424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147100-G-A

131165769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146775-C-T

131165880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146736-T-C

131165891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146725-A-G

131165894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146722-T-C

131166033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146589-G-A

131166087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146542-T-C

131166202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146458-T-A

131166228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146432-T-G

131166433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146211-T-C

131166464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146180-A-G

131166728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145913-G-A

131166728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145913-G-T

131166744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145897-A-G

http://identifiers.org/hco/6/GRCh38#131166817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25145818-C-A

131166818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145817-C-T

131166962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145496-C-G

131167109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145358-G-T

131167251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145192-C-T

131167311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145147-A-G

131167328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145130-G-C

131167413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145051-C-G

131167441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25145015-A-T

131167475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144974-T-C

131167505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144951-C-G

131167565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144889-G-C

131167572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144881-T-A

http://identifiers.org/hco/6/GRCh38#131167816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25144732-C-A

131167866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144689-C-G

131168835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143634-T-A

131168835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143634-T-G

http://identifiers.org/hco/6/GRCh38#131168867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25143606-A-C

131169117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25143360-A-G

131169145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25143332-T-A

131169243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25143234-G-A

http://identifiers.org/hco/6/GRCh38#131169246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25143231-C-A

131169249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25143228-G-A

http://identifiers.org/hco/6/GRCh38#131169292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25143171-C-A

131169330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143125-A-T

131169446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142954-T-G

131169447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142953-T-A

http://identifiers.org/hco/6/GRCh38#131169463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25142937-A-C

http://identifiers.org/hco/6/GRCh38#131169533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25142869-C-A

131169533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142869-C-T

131169591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142809-C-G

http://identifiers.org/hco/6/GRCh38#131169855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25142598-C-A

131169855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142598-C-T

131169870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142586-A-G

131169904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142553-G-A

131169917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142540-C-T

131170449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142355-C-T

131170574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142237-G-A

http://identifiers.org/hco/6/GRCh38#131171107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25140407-A-C

131171679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25139138-G-A

131171681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25139136-G-T

131171737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25139097-G-T

131171872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25138960-T-A

131173602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137624-T-C

131173931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137356-T-C

131173998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137237-G-A

131174123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137116-C-G

131174123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137116-C-T

131174133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137106-A-T

http://identifiers.org/hco/6/GRCh38#131174182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25137075-C-A

131174347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25136755-G-A

131174715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135967-G-A

http://identifiers.org/hco/6/GRCh38#131174760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25135921-A-C

131174783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135888-G-A

131175669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134834-G-A

http://identifiers.org/hco/6/GRCh38#131175729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25134737-A-C

131175729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134737-A-G

131175908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134595-C-T

131176049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134443-A-G

131176144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134231-G-T

131176228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134151-G-A

131176233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134146-G-A

131176247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134132-G-A

http://identifiers.org/hco/6/GRCh38#131176906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25133513-C-A

131177620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25133113-A-G

131177934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25132810-A-G

131178006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25132741-T-G

131187824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25129129-C-G

131187824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25129129-C-T

http://identifiers.org/hco/6/GRCh38#131188106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25127284-A-C

131188166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127217-A-G

131188178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127205-G-A

131188235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127145-A-G

131189640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25117753-A-G

131189845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25117403-C-T

http://identifiers.org/hco/6/GRCh38#131199436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115658-C-A

131199436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115658-C-G

131199436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115658-C-T

131199480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25115615-T-C

http://identifiers.org/hco/6/GRCh38#131199581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115514-C-A

131199581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25115514-C-T

http://identifiers.org/hco/6/GRCh38#131199587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115508-C-A

131199587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115508-C-T

131199591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115504-T-C

131199601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115494-G-T

131199664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115432-T-C

131199664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115432-T-G

131199679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115412-T-A

131199679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115412-T-C

http://identifiers.org/hco/6/GRCh38#131199689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115402-C-A

131199701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115390-G-T

http://identifiers.org/hco/6/GRCh38#131199706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115385-C-A

131199711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115382-C-G

131199711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25115382-C-T

http://identifiers.org/hco/6/GRCh38#131199721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115372-C-A

131199788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115315-C-T

131199862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115248-G-A

131199862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115248-G-T

http://identifiers.org/hco/6/GRCh38#131199874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115236-C-A

http://identifiers.org/hco/6/GRCh38#131199876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115234-C-A

131199891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115223-T-A

131199891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115223-T-G

131199915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115200-T-G

131199937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115171-T-A

http://identifiers.org/hco/6/GRCh38#131199941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#25115167-C-A

131199947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115162-C-G

131199947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25115162-C-T

131200397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25115030-G-T

131200427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25115000-C-G

131200654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25114764-C-T

131200658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25114760-G-T

131200755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25114677-T-C

131200978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25114464-G-A

131200995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25114440-A-G

131201076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25114352-C-G

131201202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25114247-C-G

131201242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25114207-C-T

131201330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25114138-C-T

131204312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25112194-A-T

131204515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25112031-G-A

131204610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111957-C-G

131204610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111957-C-T

131204932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111462-G-A

131205203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111238-A-G

131205208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111233-C-G

131205208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111233-C-T

131205280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111163-C-T

131205298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111145-G-A

131206940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25111010-C-G

131207050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25110917-C-T

131207133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25110840-C-T

131207147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25110819-T-C

131207465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110532-G-A

http://identifiers.org/hco/6/GRCh38#131207471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25110525-A-C

131208228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109787-T-C

131208344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109667-T-C

131209145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107932-T-C

131209146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107931-G-A

http://identifiers.org/hco/6/GRCh38#131209645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25107745-C-A

131209645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107745-C-G

131209762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107624-C-T

131209811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107565-A-G

131209838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107539-G-C

131209844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107533-A-T

131210077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107417-A-G

131210185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107309-A-G

131210213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107275-A-T

131210415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107119-A-G

131211267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106949-T-A

http://identifiers.org/hco/6/GRCh38#131211463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25106723-A-C

131211463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106723-A-T

131211476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106710-T-G

http://identifiers.org/hco/6/GRCh38#131213519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25105514-A-C

131213522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105511-A-G

131213873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105175-C-T

131213874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105174-G-A

131213885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105168-T-C

131213953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105122-T-C

131214425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104694-A-G

131215454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104095-G-C

131215560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104011-A-G

131215563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104008-G-A

131215681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103885-A-G

131215903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103678-C-G

131216069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103543-C-T

131216179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103503-A-T

131216271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103473-C-T

131216380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103365-C-T

http://identifiers.org/hco/6/GRCh38#131216389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25103356-A-C

131216447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25103293-T-C

131216466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 25103274-T-C

131216496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 25103244-C-G

131216501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25103239-A-G

131216710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25103047-T-C

131216746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25102955-A-G

131216764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25102939-G-A

131216772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25102933-T-C

131216883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25102820-T-G

131217310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25102351-T-C

131217529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25102118-G-A

http://identifiers.org/hco/6/GRCh38#131217538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25102109-A-C

131217690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25101965-T-C

131218176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25097664-C-T

131218576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25097329-A-G

http://identifiers.org/hco/6/GRCh38#131218666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25097242-A-C

131218666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25097242-A-G

131218675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25097233-C-T

131218797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25097128-G-T

131219479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096873-G-C

131219479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096873-G-T

http://identifiers.org/hco/6/GRCh38#131219540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25096770-C-A

131219571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096744-G-A

131219571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096744-G-T

http://identifiers.org/hco/6/GRCh38#131219587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25096729-A-C

131219587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096729-A-G

http://identifiers.org/hco/6/GRCh38#131219600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25096716-A-C

131219600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096716-A-G

131219600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096716-A-T

131219621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25096696-G-T

131219682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 25096633-G-T

131219775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25096540-G-C

131219775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25096540-G-T

131219796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25096519-T-C

131219840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25096474-T-C

131219917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25096388-T-C

131220266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25096101-C-T

http://identifiers.org/hco/6/GRCh38#131220416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25095940-A-C

131220473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095884-A-T

http://identifiers.org/hco/6/GRCh38#131220526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25095834-A-C

131220526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095834-A-G

131223354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095687-C-T

131223378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095660-T-A

131223455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095595-G-T

131223591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095460-A-T

131223715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095373-T-G

131223859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095235-A-G

131223859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095235-A-T

131223961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25095156-C-T

131226440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25093106-C-T

131226619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25092955-G-A

131226667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25092916-T-G

131226759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25092827-C-T

131227961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25090491-T-C

131227961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25090491-T-G

131228027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25090435-G-C

131228209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089875-A-G

131228462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089629-A-G

http://identifiers.org/hco/6/GRCh38#131228651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25089583-A-C

131228734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089517-G-A

131228818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089442-C-T

131228827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089433-A-G

131228873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089387-A-G

131229152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089066-C-T

131229173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089036-T-C

131229195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25089014-C-T

131230777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25088319-T-G

131230783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25088313-G-A

131230979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25088142-A-G

131231322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25087832-G-T

131231614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087558-A-G

131231875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087269-T-G

131231968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25087178-A-G

131231968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25087178-A-T

131232082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25087065-G-A

131232082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25087065-G-C

131232251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25086887-G-A

131232328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25086815-A-G

131232868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25085969-T-G

131233233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25084861-G-A

131233271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25084819-G-C

131233410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25084633-A-G

131244247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25084158-C-T

131244484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083945-C-T

131244748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083577-G-A

131244881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083451-T-C

131245288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083091-C-T

131245359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083038-C-G

131245359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083038-C-T

http://identifiers.org/hco/6/GRCh38#131245390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25083011-A-C

131245536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25082843-G-A

http://identifiers.org/hco/6/GRCh38#131245537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25082842-C-A

131245696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25082409-A-G

131246060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25081944-C-T

131246159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25081847-T-C

http://identifiers.org/hco/6/GRCh38#131246363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25081656-C-A

131246668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080513-G-T

131246699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080483-T-A

131246943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080308-T-A

131247116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080152-G-C

131247775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078667-G-A

131248122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078379-G-A

131248373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078145-T-C

131248620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078019-G-A

131248876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077793-G-T

131249121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077513-G-T

131249552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25076886-C-T

131250050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25076396-T-C

131250111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25076336-T-A

131250229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25076207-T-C

131250296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25076151-G-A

131250296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25076151-G-T

http://identifiers.org/hco/6/GRCh38#131250416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25076042-C-A

http://identifiers.org/hco/6/GRCh38#131250541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25075949-C-A

131250635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075883-G-A

131250641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075877-A-G

131250844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075730-C-G

131251102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075476-C-T

131251202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075347-A-G

131251529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075020-T-A

131251582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074971-A-G

131251616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074934-G-C

131251746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074821-T-C

131251844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074737-G-T

131251848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074733-A-G

131251854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074727-C-T

131251959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074626-G-A

131251968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074617-A-T

131252136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074463-G-T

131252166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074433-G-C

131252261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074335-G-A

131252284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074310-A-G

131252368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074231-T-A

131252669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074019-G-A

131252669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074019-G-C

131252675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074013-A-G

131252811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073868-T-C

131253005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073662-T-G

131253036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 25073631-G-C

131253062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 25073605-A-G

131254102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073286-T-G

131254307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073074-G-C

131254330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073051-T-C

131254632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25072798-C-T

131254633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25072797-A-G

131254635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25072795-T-C

http://identifiers.org/hco/6/GRCh38#131254688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25072757-A-C

131255943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070986-A-G

131255944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070985-T-C

131255945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070984-G-C

131256024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070906-T-C

131256069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25070861-C-T

131257208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25069200-T-C

http://identifiers.org/hco/6/GRCh38#131257419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25069161-C-A

131257785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068924-G-A

131257801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068921-G-C

131257992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068694-G-T

http://identifiers.org/hco/6/GRCh38#131258570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25068027-A-C

131258705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067931-T-C

131259308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067351-A-T

131261695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064968-T-C

131262055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064648-C-T

131262116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064587-A-G

131262202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063070-G-A

131262350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25062942-T-C

131262420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25062872-T-A

131262529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25062761-A-T

131262661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25062639-C-T

http://identifiers.org/hco/6/GRCh38#131262889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25061917-A-C

131262893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25061913-G-C

131262937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25061871-A-G

131263768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060882-G-C

131263983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060713-G-A

131264013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060682-T-A

131264013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060682-T-C

131264329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060326-A-G

131265495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059748-G-A

131265603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059671-T-C

131265645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059629-A-G

131265741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059542-T-C

131265888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059401-G-A

131265891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059398-C-T

131265897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059392-C-T

http://identifiers.org/hco/6/GRCh38#131266006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25059327-C-A

http://identifiers.org/hco/6/GRCh38#131266013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25059320-C-A

131266013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059320-C-G

131266579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058856-A-G

131266798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058677-G-T

131267269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057806-T-C

131267343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057746-T-C

131267519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057596-A-G

http://identifiers.org/hco/6/GRCh38#131267539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25057576-C-A

131267603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057518-C-T

131267850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056518-A-G

131267904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056469-G-T

131267998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056365-G-A

131268112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056252-T-C

http://identifiers.org/hco/6/GRCh38#131268129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25056235-A-C

http://identifiers.org/hco/6/GRCh38#131268263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25056113-A-C

http://identifiers.org/hco/6/GRCh38#131268266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25056110-A-C

131268276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056100-C-T

131268298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056079-A-G

131268431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055960-C-T

131268432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055959-G-A

http://identifiers.org/hco/6/GRCh38#131268460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25055932-A-C

131268471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055921-T-G

131268718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055683-G-T

131269416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055332-G-C

131269446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055303-T-C

131269597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055158-A-G

131269868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054903-A-T

http://identifiers.org/hco/6/GRCh38#131269869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25054902-A-C

131269869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054902-A-G

131269925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054850-G-A

131269925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054850-G-T

131270065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054726-A-G

http://identifiers.org/hco/6/GRCh38#131270252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25054544-C-A

131270252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054544-C-G

131270386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054398-C-G

131270568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054227-T-C

131270691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25054115-A-G

131276909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052229-G-A

131276922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052216-C-T

http://identifiers.org/hco/6/GRCh38#131277114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25052015-C-A

131277158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051965-T-A

131277168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051955-T-C

131277370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051456-T-C

131277414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051412-A-G

131277678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051146-G-T

131277752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25050974-T-C

http://identifiers.org/hco/6/GRCh38#131277817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25050864-A-C

131277944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25050742-A-G

131278150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25050513-G-T

131278894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049739-T-C

131279110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049264-C-G

131279110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049264-C-T

131279125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049249-A-G

131279128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049246-A-G

http://identifiers.org/hco/6/GRCh38#131279247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25049133-A-C

131279836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25048740-T-A

131280011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25048566-A-T

131280293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25048332-C-T

131280362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25048269-G-A

131280385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25048245-C-T

131280430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25048201-C-T

131280844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25047831-A-G

131280854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25047821-C-G

131280986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25047686-C-G

131280986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25047686-C-T

131281212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25047456-G-T

131281286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25047383-C-T

131281307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25047362-G-A

http://identifiers.org/hco/6/GRCh38#131281496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25047176-C-A

131281598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25047076-G-A

131281610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25047064-G-C

http://identifiers.org/hco/6/GRCh38#131281652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25047022-C-A

131281652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25047022-C-G

131281652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25047022-C-T

http://identifiers.org/hco/6/GRCh38#131281728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046946-C-A

131281728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046946-C-T

http://identifiers.org/hco/6/GRCh38#131281774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046920-C-A

131281781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046913-T-C

131281871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046834-G-C

131281885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046819-G-A

131281885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046819-G-T

http://identifiers.org/hco/6/GRCh38#131281922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046783-C-A

131281922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046783-C-T

http://identifiers.org/hco/6/GRCh38#131281962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046746-C-A

http://identifiers.org/hco/6/GRCh38#131281972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046736-C-A

131281972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046736-C-T

http://identifiers.org/hco/6/GRCh38#131281976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046732-C-A

131281976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046732-C-T

131281989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046719-A-G

131282005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046703-A-G

http://identifiers.org/hco/6/GRCh38#131282204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046510-C-A

131282204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046510-C-T

131282224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046490-G-C

131282257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046459-T-C

131282349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046369-T-A

131282349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046369-T-G

131282508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046189-G-C

131282546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046151-G-T

http://identifiers.org/hco/6/GRCh38#131282616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046082-C-A

131282616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25046082-C-T

http://identifiers.org/hco/6/GRCh38#131282628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25046067-C-A

http://identifiers.org/hco/6/GRCh38#131282718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25045980-C-A

131282718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045980-C-T

131282824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045828-G-C

131282824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045828-G-T

131282843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045809-T-C

http://identifiers.org/hco/6/GRCh38#131282845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25045807-C-A

131282845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045807-C-T

131282861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045791-G-T

http://identifiers.org/hco/6/GRCh38#131282959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25045604-C-A

131282959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045604-C-T

131282962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045601-T-A

131283252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045287-T-G

131283281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045258-G-T

131283355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25045170-G-T