131092566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137810877-T-G

131092575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137810886-C-T

131092576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137810887-C-T

131092624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137810931-A-G

131092684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137810990-C-T

131092697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137811003-C-T

http://identifiers.org/hco/10/GRCh38#131092702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137811008-A-C

http://identifiers.org/hco/10/GRCh38#131092792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137811079-A-C

131092792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137811079-A-G

131092796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137811083-T-A

131092796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137811083-T-G

http://identifiers.org/hco/10/GRCh38#131092911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137811196-A-C

http://identifiers.org/hco/10/GRCh38#131093077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137811359-A-C

131093077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137811359-A-G

131093122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137811379-C-G

131093122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137811379-C-T

131093282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137811540-C-T

131093321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137811579-G-A

http://identifiers.org/hco/10/GRCh38#131093330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137811588-A-C

131093330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811588-A-T

131093345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811607-A-G

131093439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811663-G-A

131093439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811663-G-C

131093439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811663-G-T

131093559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811748-G-A

http://identifiers.org/hco/10/GRCh38#131093608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137811777-A-C

131093788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811912-T-C

131093788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811912-T-G

131093829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811953-G-A

131093836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137811960-T-C

131093954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812064-C-T

http://identifiers.org/hco/10/GRCh38#131093968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137812076-A-C

131093968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812076-A-G

131094019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812128-G-A

131094031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812140-G-A

http://identifiers.org/hco/10/GRCh38#131094045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137812155-C-A

131094067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812178-G-A

131094067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812178-G-T

131094150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812260-G-A

131094247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812347-C-T

131094258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812358-C-T

131094324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812445-T-C

131094455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137812571-T-C

131094605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812697-A-G

131094620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137812712-T-C

131095730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137813390-T-G

131095811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137813469-G-A

131095811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137813469-G-T

http://identifiers.org/hco/10/GRCh38#131095837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137813494-C-A

131095837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137813494-C-T

131095866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137813529-T-C

131098268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815024-A-G

131098286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815042-G-T

131098311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137815067-A-G

131098488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815245-T-C

131098489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815246-C-G

http://identifiers.org/hco/10/GRCh38#131098547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137815298-C-A

http://identifiers.org/hco/10/GRCh38#131098569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137815319-C-A

131098633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815369-C-T

131098878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815596-T-C

131098896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137815613-A-T

131098902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137815619-T-C

131098906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815623-C-T

131098914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815631-T-A

131098938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815654-T-C

131098942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815658-A-G

131099083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815822-C-T

131099103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815915-T-C

131099111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137815923-T-C

131099208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137816169-C-T

131099262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137816222-C-T

131099624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137816649-G-A

131100255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137816955-A-G

131100471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137817167-C-T

131100544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137817237-G-T

http://identifiers.org/hco/10/GRCh38#131100884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137817543-C-A

131101075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137817715-G-A

131101264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137817926-G-A

131101338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137817993-C-G

131101338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137817993-C-T

131102102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137818394-A-G

http://identifiers.org/hco/10/GRCh38#131104130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137819667-C-A

131104130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137819667-C-T

131104310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137819787-C-T

131104392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137819869-T-C

131104413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137819889-C-T

131104426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137819902-A-G

131104485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137819969-T-C

131104756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137820239-T-C

131109206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137823444-T-C

131109813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137823846-T-G

131109835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137823866-G-C

131109930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137823952-C-T

131110053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824068-G-A

131110488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824514-C-G

131110488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824514-C-T

131110682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824687-C-T

131110683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824688-G-A

131110683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824688-G-T

http://identifiers.org/hco/10/GRCh38#131110859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137824858-C-A

131110903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824900-G-A

131110903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824900-G-C

131110950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824973-C-T

131110955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137824978-C-T

http://identifiers.org/hco/10/GRCh38#131111062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137825067-A-C

131111243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137825212-T-C

131111261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137825227-G-A

131111278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137825244-T-A

131111681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137825612-C-T

131111802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137825732-G-T

131111958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137825847-C-T

131111990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137825863-A-T

131113716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137828876-C-T

131114423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137829529-G-C

131114514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137829565-C-T

131114515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137829566-G-A

131114549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137829603-T-C

131115630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137830761-C-G

131115736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137830859-C-T

131115759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137830883-C-T

131115766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137830890-G-T

131116021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137831120-C-T

131116022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137831121-G-A

131116177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137831274-G-A

131116280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137831347-G-A

http://identifiers.org/hco/10/GRCh38#131116485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137831507-C-A

131116485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137831507-C-T

http://identifiers.org/hco/10/GRCh38#131116805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137831575-C-A

131116805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137831575-C-G

131116805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137831575-C-T

http://identifiers.org/hco/10/GRCh38#131116808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137831578-C-A

131116808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137831578-C-T

http://identifiers.org/hco/10/GRCh38#131116923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137831693-C-A

131116923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137831693-C-T

131116962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137831733-A-G

http://identifiers.org/hco/10/GRCh38#131116963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137831734-C-A

131116963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137831734-C-T

131119217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137832755-T-A

131119217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137832755-T-G

131119290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137832826-G-A

131119401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137832937-T-C

131119642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833112-C-G

131119642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833112-C-T

131119643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833113-G-A

131119804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833273-C-T

http://identifiers.org/hco/10/GRCh38#131119814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137833281-C-A

http://identifiers.org/hco/10/GRCh38#131119832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137833296-C-A

131119833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833297-C-T

131119893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833349-C-T

131119917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833377-G-C

131119990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833460-G-A

http://identifiers.org/hco/10/GRCh38#131120017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137833482-C-A

131120028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833498-T-C

131120461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833646-C-T

131120476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137833661-C-G

131120921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834017-G-C

131120936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834030-A-T

http://identifiers.org/hco/10/GRCh38#131120958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137834049-C-A

131120982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834075-G-A

131121084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834176-T-C

http://identifiers.org/hco/10/GRCh38#131121098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137834190-C-A

131121098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834190-C-T

131121233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834285-A-G

131121259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834310-A-G

131121318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834399-C-T

131121360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834442-C-T

131121391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834473-A-G

131121407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834489-C-T

131121418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137834496-C-T

131122905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835381-T-C

131122909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835386-T-G

131122928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835405-G-C

131123010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835470-G-A

131123239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835689-A-G

131123255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835696-C-T

131123283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835719-A-G

131123351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835782-A-T

131123409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835817-T-G

http://identifiers.org/hco/10/GRCh38#131123559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137835942-A-C

131123561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137835944-C-G

131123656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137836026-C-T

131123747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137836105-G-A

131123834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137836175-G-A

131123966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137836294-G-A

131124009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137836337-A-T

http://identifiers.org/hco/10/GRCh38#131124339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137837499-A-C

131124422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137837569-T-C

131124634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137837776-C-T

131124773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137837893-G-A

131124777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137837897-G-A

131124936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137838064-T-C

131124939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137838066-G-T

131125102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137838359-G-A

131125689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839123-G-A

131125724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839159-A-G

131125988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839362-C-T

131126135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839467-C-T

131126472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839929-G-C

131126501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839958-C-T

131126525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839973-C-T

131126538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137839986-A-T

131126584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840035-C-T

131126605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840056-G-A

131126605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840056-G-C

131126613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840064-C-T

131126651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840085-A-G

http://identifiers.org/hco/10/GRCh38#131126670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137840104-A-C

131126697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840126-G-A

131126720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840146-T-C

http://identifiers.org/hco/10/GRCh38#131126759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137840185-C-A

131126759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840185-C-T

131126809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840225-G-A

131126902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840281-A-G

131127028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840394-C-T

131127197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840644-C-G

131127197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840644-C-T

131127292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137840709-A-T

131131843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137847936-G-A

131132349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137848566-C-T

131132570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137848686-C-T

http://identifiers.org/hco/10/GRCh38#131132853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137848977-C-A

131132956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849070-A-G

131133098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849192-T-G

131133203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849272-C-T

131133391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849439-G-A

131133600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849507-C-G

http://identifiers.org/hco/10/GRCh38#131133748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137849659-A-C

131133748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849659-A-T

131134216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849956-C-T

131134253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137849980-C-T

http://identifiers.org/hco/10/GRCh38#131134256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137849983-C-A

131134287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137850018-T-C

131134312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137850038-T-G

131134420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137850142-T-A

131134420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137850142-T-C

131134420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137850142-T-G

http://identifiers.org/hco/10/GRCh38#131134432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137850154-C-A

131134432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137850154-C-T

131134438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137850160-G-A

131134438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137850160-G-T

http://identifiers.org/hco/10/GRCh38#131134508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#137850227-C-A

131134933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137850622-T-A

131134975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137850661-C-T

131135077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137850760-G-A

131141076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137853994-G-A

131141244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854156-T-A

131141392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854291-C-T

131141720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854551-T-G

131141849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854667-C-T

131141886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854705-T-C

131141908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854727-C-T

131141921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854743-C-T

131141927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854749-C-T

131141946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854768-G-T

131142003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854839-G-C

131142004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854840-G-A

131142009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854845-T-C

131142058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854888-C-T

131142059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854889-G-A

131142059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854889-G-C

131142120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137854944-A-T

131142617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137855400-G-A

131142773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137855548-C-T

131142845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137855623-C-T

http://identifiers.org/hco/10/GRCh38#131142945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137855725-C-A

http://identifiers.org/hco/10/GRCh38#131142959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137855742-C-A

131142959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137855742-C-T

131142962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137855745-G-C

131143146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137855942-C-T

131143224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137856020-C-T

131143245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137856048-T-C

131143245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137856048-T-G

131143503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137856274-G-C

131143612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137856383-G-C

131143647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137856416-C-G

http://identifiers.org/hco/10/GRCh38#131143733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137856489-C-A

131144812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137859761-C-T

131145277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137860176-C-T

131145363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137860256-A-G

131145422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137860329-A-G

131145461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137860369-G-A

131145891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137860974-T-A

131146037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861108-C-T

131146063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861142-T-C

131146198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861256-G-A

131146294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861319-A-G

131146356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861380-T-C

131146356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861380-T-G

131146378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861401-G-A

131146378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861401-G-T

http://identifiers.org/hco/10/GRCh38#131146411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137861434-A-C

131146411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861434-A-G

131146645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137861666-C-T

http://identifiers.org/hco/10/GRCh38#131146728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137861745-A-C

131146728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861745-A-G

131146728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861745-A-T

131146786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861786-G-A

131146786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137861786-G-T

131147089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137862050-A-G

131147534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137862291-G-C

131147736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137862479-C-T

131147788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137862520-C-T

131147973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137862660-C-T

131148166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137862836-A-G

http://identifiers.org/hco/10/GRCh38#131148267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137862917-A-C

131148328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137862951-A-G

http://identifiers.org/hco/10/GRCh38#131148449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137863072-C-A

131148449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137863072-C-T

131148453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137863076-T-C

131150005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137868992-T-C

131150115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137869103-G-A

131153093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137870592-G-A

131153148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137870656-A-G

131153423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137870839-A-G

131153544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137870936-C-T

131153620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137871016-G-A

131153749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137871151-T-C

131154094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137871497-T-C

131154689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872058-G-A

131154708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872086-A-G

131155059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872332-A-G

http://identifiers.org/hco/10/GRCh38#131155171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137872454-C-A

131155171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872454-C-T

131155220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872491-G-A

131155220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872491-G-C

131155320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872595-A-G

131155403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872654-A-T

131155494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872706-C-T

131155583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872785-T-C

131155696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137872895-C-T

131155915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137873100-C-T

http://identifiers.org/hco/10/GRCh38#131155947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137873133-C-A

http://identifiers.org/hco/10/GRCh38#131156010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137873196-C-A

131156010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137873196-C-T

131156040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137873226-C-T

http://identifiers.org/hco/10/GRCh38#131156060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137873244-C-A

131156060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137873244-C-T

http://identifiers.org/hco/10/GRCh38#131156206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137873390-C-A

http://identifiers.org/hco/10/GRCh38#131156329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137873513-C-A

131156473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137873635-C-T

http://identifiers.org/hco/10/GRCh38#131157656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137874217-A-C

131157705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137874240-T-G

131157746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137874259-G-A

131158192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137874659-T-C

131158309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137874772-G-A

131158313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137874776-A-G

131159423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137875416-T-A

131159423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137875416-T-C

131159637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137875638-C-T

131159710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137875739-G-A

131159801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137875876-C-T

131159840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137875903-C-G

131159921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137875988-A-G

131159993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876065-C-T

131160058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876151-C-G

131160169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876261-T-C

131160203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876297-G-A

131160670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876658-G-A

131160670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876658-G-T

131160673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876661-G-A

131160673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876661-G-T

http://identifiers.org/hco/10/GRCh38#131160685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137876675-C-A

131160685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876675-C-G

131160685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876675-C-T

131160694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876683-G-A

131160694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876683-G-T

131160720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137876709-T-C

131161894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877023-C-T

131162030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877163-C-T

http://identifiers.org/hco/10/GRCh38#131162501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137877707-C-A

131162501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877707-C-G

131162501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877707-C-T

http://identifiers.org/hco/10/GRCh38#131162502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137877708-A-C

131162502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877708-A-G

131162519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877724-G-T

131162520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877725-G-T

131162524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877729-T-C

131162531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877736-T-G

http://identifiers.org/hco/10/GRCh38#131162540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137877745-A-C

131162545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877751-G-T

131162739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877948-A-G

131162739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137877948-A-T

131162790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878000-T-C

131162791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878001-G-T

131162818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878027-A-G

131162842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878052-T-G

http://identifiers.org/hco/10/GRCh38#131162846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878056-C-A

131162846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878056-C-T

http://identifiers.org/hco/10/GRCh38#131162915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878121-C-A

http://identifiers.org/hco/10/GRCh38#131162965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878168-C-A

131162965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878168-C-T

131162966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878169-C-T

131162970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878173-G-A

131162970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137878173-G-T

131162991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137878194-G-T

131162999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878202-A-G

131163028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878229-T-A

131163028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878229-T-C

131163038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878239-G-A

131163038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878239-G-T

http://identifiers.org/hco/10/GRCh38#131163080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878281-C-A

131163080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878281-C-G

131163080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878281-C-T

131163082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878283-A-G

131163099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878292-T-C

131163104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878297-G-A

131163104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878297-G-T

131163111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878304-G-A

131163111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878304-G-T

http://identifiers.org/hco/10/GRCh38#131163196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878389-C-A

131163196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137878389-C-T

131163230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878421-G-A

131163230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878421-G-T

http://identifiers.org/hco/10/GRCh38#131163254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878456-A-C

http://identifiers.org/hco/10/GRCh38#131163255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878457-C-A

http://identifiers.org/hco/10/GRCh38#131163294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878495-A-C

131163306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878508-G-A

131163306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878508-G-T

http://identifiers.org/hco/10/GRCh38#131163429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137878642-C-A

131163439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878652-C-T

131163565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137878760-G-C

131164163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879197-G-A

131164163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879197-G-T

131164170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879204-T-A

131164170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879204-T-C

131164182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879221-T-A

131164214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879253-G-C

131164214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879253-G-T

131164634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879669-G-A

131164693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137879727-G-A

131165445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137880790-G-A

131165537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137880855-C-G

131165796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 137881173-C-T

131166018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137881391-G-T

http://identifiers.org/hco/10/GRCh38#131166657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137881609-C-A

131166657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137881609-C-T

http://identifiers.org/hco/10/GRCh38#131166675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137881622-C-A

131166675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137881622-C-T

131166688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137881638-A-T

131166914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137881854-A-G

131166947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137881888-G-T

131167000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137881933-T-C

131167313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137882266-C-T

131167394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137882347-G-A

131167401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137882354-A-G

131167423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137882375-C-T

131167519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137882457-C-T

131167560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137882498-G-T

131168261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883343-G-C

131168299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883388-C-T

131168308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883394-A-G

http://identifiers.org/hco/10/GRCh38#131168444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137883521-C-A

131168444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883521-C-T

131168456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883533-C-G

131168500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883564-T-G

131168530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883585-G-C

131168560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883618-C-T

131168561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883619-C-T

131168720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883822-C-T

131168752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883854-G-A

131168752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883854-G-C

131168756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883858-G-A

131168793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137883900-C-T

http://identifiers.org/hco/10/GRCh38#131169297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137885755-C-A

131169626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137886092-G-C

131169813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137886237-A-G

http://identifiers.org/hco/10/GRCh38#131169930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137886352-A-C

131170702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137887095-G-T

131174586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137887587-T-C

131175376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888174-G-A

131175507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888304-A-G

131175567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888366-C-T

131175660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888455-T-C

http://identifiers.org/hco/10/GRCh38#131175773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137888554-C-A

http://identifiers.org/hco/10/GRCh38#131175783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137888564-A-C

131175907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888664-A-G

131175911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888668-G-A

131175961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888702-T-A

131176176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888908-C-T

http://identifiers.org/hco/10/GRCh38#131176214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137888947-C-A

131176214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888947-C-T

131176313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137888980-T-G

http://identifiers.org/hco/10/GRCh38#131176453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137889082-C-A

131176463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889092-C-T

131176499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889126-C-T

131176534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889157-G-A

131176653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889275-T-G

131176687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889312-C-T

131176699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889322-G-A

131176748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889362-A-G

131176760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889372-A-G

131176803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889415-C-T

131177996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889580-G-T

131178019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137889608-G-A

131180562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137891663-A-G

131180597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137891698-C-G

131180666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137891765-T-C

http://identifiers.org/hco/10/GRCh38#131181091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137892168-C-A

131181091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892168-C-G

131181127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892202-A-G

http://identifiers.org/hco/10/GRCh38#131181185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137892228-A-C

131181213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892253-G-C

131181215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892255-G-A

131181453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892493-A-G

131181488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892519-T-C

131182491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892800-T-G

131182609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137892918-T-C

131183099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137893395-G-A

http://identifiers.org/hco/10/GRCh38#131183204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137893494-A-C

131183208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137893502-G-C

131183320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137893600-T-C

131183557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137893834-T-C

131183651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137893902-C-T

131183672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137893923-C-T

http://identifiers.org/hco/10/GRCh38#131183692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137893942-C-A

131183692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137893942-C-T

131183888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137894049-C-T

131184281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137894394-A-G

131184459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137894577-A-G

131187800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137895614-G-A

131187880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137895699-G-A

131187880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137895699-G-T

http://identifiers.org/hco/10/GRCh38#131188426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137896246-C-A

131188426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896246-C-T

131188562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896381-T-G

131188607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896429-G-T

131188671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896490-T-C

http://identifiers.org/hco/10/GRCh38#131188823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137896611-A-C

131188823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896611-A-G

131188823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896611-A-T

131188897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896680-G-A

131188897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896680-G-C

131188897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137896680-G-T

131201322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899236-G-T

131201367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899276-T-C

131201403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899314-C-T

131201437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899348-G-A

131201588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899447-T-A

131201721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899560-A-T

131201729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899568-C-T

131201767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137899605-G-A

131202979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137901115-G-C

131204915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137903321-G-C

131205188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137903577-C-T

131205422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137903791-T-C

131205566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137903935-T-A

131205568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137903937-T-C

131205763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137904114-C-T

131205773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137904124-C-G

131205833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137904147-G-A

131205833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137904147-G-C

131206553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137904663-G-C

131206573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137904683-A-T

131206626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137904738-C-T

http://identifiers.org/hco/10/GRCh38#131209317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137905706-A-C

131209368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137905758-C-T

131209373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137905763-T-C

131210045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137906468-G-C

131210078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137906503-T-G

131210183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137906580-A-G

131210345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137906713-G-A

131210589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137906941-G-T

131210684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907086-C-T

131211081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907540-C-T

131211372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907744-A-T

131211457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907794-C-G

131211457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907794-C-T

131211458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907795-G-A

131211465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907802-G-C

131211513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907852-C-G

131211588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137907935-C-T

131212174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137909606-T-A

131212462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137909918-T-G

131213045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137910519-C-T

131213719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911072-G-A

131213720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911073-C-T

131214834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911529-C-T

131214937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911598-C-T

131214975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911633-T-C

131215034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911694-G-A

131215094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911745-T-C

131215119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911769-C-T

131215162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911812-T-C

131215257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137911919-G-A

131215352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137912012-A-G

131215702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137912723-C-T

131215772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137912797-C-T

131216050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137913048-A-T

131216125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137913088-C-T

131216199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137913167-T-C

131221347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137927935-C-T

131221364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137927952-C-T

131221365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137927953-A-G

131221417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137928009-A-G

131221675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137928240-T-C

131221857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137928390-T-C

131221891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137928407-G-A

131221965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137928488-G-A

131221965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137928488-G-C

131222293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137928769-T-C

131225321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137929784-G-A

131225379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137929841-G-C

131225405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137929866-C-T

131225500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137929950-T-C

http://identifiers.org/hco/10/GRCh38#131225558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137929998-A-C

131225568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930008-C-T

http://identifiers.org/hco/10/GRCh38#131225600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137930044-A-C

131225643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930088-C-T

131225674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930116-T-A

131225733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930168-A-G

131225733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930168-A-T

http://identifiers.org/hco/10/GRCh38#131226460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137930414-C-A

131226460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930414-C-T

131226481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930435-T-A

131226871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930831-T-C

131227025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137930971-T-A

131227219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931152-G-C

131227560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931451-C-T

131227618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931487-T-C

131227618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931487-T-G

131227658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931525-C-T

131227876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931769-A-T

131227972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931906-C-T

131227974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931908-C-G

131228010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931936-G-A

131228010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931936-G-T

131228019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137931945-G-C

131233514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137935958-A-T

131233674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137936106-T-C

131234310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137936288-T-G

131234313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137936291-G-C

131235087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137936682-C-T

131235112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137936706-C-T

http://identifiers.org/hco/10/GRCh38#131235113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137936707-A-C

131235139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137936731-G-A

131235544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137937115-T-C

131235599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137937155-A-G

131235915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137937571-C-G

131236017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137937884-G-A

131236063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137937936-G-A

131236150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938019-T-C

131236363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938224-G-T

131236366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938227-A-G

131236739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938514-C-T

131236844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938618-G-T

131236861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938635-G-C

131237051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938796-C-G

131237153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938892-C-T

131237171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137938914-T-C

http://identifiers.org/hco/10/GRCh38#131237592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137939339-A-C

131238870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941582-G-A

131238876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941588-G-A

131238919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941636-C-G

131238919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941636-C-T

131238933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941650-C-G

131238933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941650-C-T

131239030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941735-C-T

131239031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941736-G-A

131239233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941929-G-A

131239233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137941929-G-T

131239381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942072-T-C

131239508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942184-G-A

131239581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942252-A-G

131239592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942263-G-T

131239619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942296-G-C

131239671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942359-G-A

131239745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942433-C-T

http://identifiers.org/hco/10/GRCh38#131239772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137942460-C-A

131239772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942460-C-G

131239772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942460-C-T

131239784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942472-C-T

131239943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942593-G-C

131240037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942645-G-A

131240141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942737-C-T

131240218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942831-A-G

131240280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942887-T-C

131240386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137942967-G-C

131240456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137943034-C-T

131240498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137943065-A-G

131242822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137943358-C-T

131242883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137943419-A-G

131242975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137943548-C-T

131243033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137943610-T-C

131243257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137943798-G-A

http://identifiers.org/hco/10/GRCh38#131245011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137947175-C-A

131245032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137947196-C-G

131245110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137947326-T-C

131245446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137947655-C-T

131255663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137958759-A-G

131255686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137958786-G-A

131255810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137958869-C-T

131255955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137959015-G-A

131256548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137959612-A-G

131256597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137959661-T-C

131257315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137960306-A-G

131257509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137960483-G-A

131257511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137960485-G-A

http://identifiers.org/hco/10/GRCh38#131258186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137961069-A-C

131258376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137961629-C-T

http://identifiers.org/hco/10/GRCh38#131258445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137961721-C-A

131258862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137961773-T-G

131258970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137961856-T-G

131259033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137961910-T-C

131259232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137962096-G-A

131259298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137962209-G-C

131259324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137962235-A-G

131259526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 137962689-A-G

131259678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137962842-G-A

131259702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137962865-G-A

131259755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137962905-C-T

131259837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137962986-G-A

http://identifiers.org/hco/10/GRCh38#131260108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137963233-A-C

http://identifiers.org/hco/10/GRCh38#131260114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137963239-A-C

131260114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963239-A-G

131260134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963259-T-C

http://identifiers.org/hco/10/GRCh38#131260142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137963266-C-A

131260142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963266-C-T

131260164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963289-A-G

http://identifiers.org/hco/10/GRCh38#131260165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137963290-C-A

131260165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963290-C-T

131260191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963308-T-A

131260191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963308-T-C

131260191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963308-T-G

http://identifiers.org/hco/10/GRCh38#131260272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137963420-C-A

131260272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137963420-C-G

131260272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137963420-C-T

131260280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137963428-G-A

131260280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137963428-G-T

131260375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: 137963535-G-A

131260375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: 137963535-G-T

http://identifiers.org/hco/10/GRCh38#131260376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137963536-C-A

131260376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: 137963536-C-T

131260437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: synonymous variant
orthologous variants: 137963600-G-A

http://identifiers.org/hco/10/GRCh38#131260469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137963629-C-A

131260469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137963629-C-T

131260595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137963729-G-A

131260598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137963732-C-T

131260709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137963809-G-A

131260727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137963826-G-C

131260728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137963827-G-C

131270062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137967374-T-A

131270062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137967374-T-C

131270276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137967602-C-T

131270301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137967629-C-T

131270387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137967723-C-T

131271756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137969499-T-G

131271837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137969571-T-C

131271960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137969672-G-A

131271963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137969675-T-C

131272146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137969819-C-T

131272336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137969984-G-A

http://identifiers.org/hco/10/GRCh38#131272446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137970093-C-A

131272596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137970228-T-C

131272620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137970253-C-T

131272735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137970370-T-A

131272735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137970370-T-C

131275209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137972631-T-G

131275438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137972938-G-A

131275641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137973131-G-A

131276281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137974241-T-C

131276646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137974578-T-C

131277110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975001-T-A

131277128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975019-C-T

131277214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975123-G-A

131277265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975169-T-C

http://identifiers.org/hco/10/GRCh38#131277385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137975283-C-A

http://identifiers.org/hco/10/GRCh38#131277488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137975369-C-A

http://identifiers.org/hco/10/GRCh38#131280844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137975518-A-C

131280889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975563-G-A

131280912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975585-A-G

131281295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975928-C-G

131281295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975928-C-T

131281342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975974-A-T

131281357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137975989-T-G

131282182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976266-G-A

131282269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976352-A-T

131282337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976420-T-A

131282337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976420-T-C

131282338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976421-G-A

131282385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976466-A-G

131282463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976542-C-T

131282478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976557-C-G

131282478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976557-C-T

131282498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976576-G-T

http://identifiers.org/hco/10/GRCh38#131282504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137976582-C-A

131282504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976582-C-T

131282543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976618-T-C

131282655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976723-A-G

131282738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976790-C-G

131282765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976816-C-G

131282840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976877-G-C

131282850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976887-G-A

131282850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137976887-G-T

http://identifiers.org/hco/10/GRCh38#131282935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137976972-A-C

http://identifiers.org/hco/10/GRCh38#131282984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137977019-A-C

131283034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977093-A-G

131283091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977149-C-T

131283093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977151-C-T

131283147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977271-T-A

131283169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977296-A-G

131283234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977360-G-T

131283235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977361-A-T

131283249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977375-C-T

131283289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977410-A-T

131283384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977524-C-T

131283439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977570-C-T

131283441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977571-G-A

131283532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137977623-C-G

http://identifiers.org/hco/10/GRCh38#131293825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137984740-C-A

131293926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137984835-C-T

http://identifiers.org/hco/10/GRCh38#131299706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137989358-A-C

131299798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137989454-C-T

131299880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137989545-C-G

131299953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137989615-T-C

131299994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137989646-G-A

131300174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137989955-A-G

131300216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990001-T-C

131300244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990025-T-C

131300418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990192-C-T

131300432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990206-G-A

131300581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990352-C-T

131300647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990400-A-G

131300821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990538-T-C

131300868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990585-G-C

131300976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990685-T-C

131301083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990787-T-C

131301236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990864-T-C

131301255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990873-G-A

131301266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137990884-G-C

131301874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137991387-C-T

131301989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137991498-A-T

131304472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137992522-C-T

131304535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137992565-G-A

131304710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137992726-G-A

131304950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137992939-T-G

131304979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137992960-T-C

131305190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137993154-C-T

131305305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137993253-C-T

131305370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137993316-T-C

http://identifiers.org/hco/10/GRCh38#131305434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137993376-A-C

http://identifiers.org/hco/10/GRCh38#131305466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137993407-C-A

http://identifiers.org/hco/10/GRCh38#131305586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137993525-C-A

131305586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137993525-C-G

131305586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137993525-C-T

131306162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137994093-A-G

131306162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137994093-A-T

131306387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137994304-T-C

http://identifiers.org/hco/10/GRCh38#131306696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137994450-A-C

131306828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137994554-A-G

131307181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137994803-C-T

131307345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137994969-C-G

131307364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137994988-A-G

131307532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995157-G-A

131307692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995332-T-A

131307775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995411-G-A

131307795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995436-A-G

131307931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995564-T-C

http://identifiers.org/hco/10/GRCh38#131308021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137995650-C-A

131308070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995703-G-T

131308075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995708-A-G

131308112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995752-T-C

131308114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995754-T-A

131308114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995754-T-C

131308126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995766-G-C

131308126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137995766-G-T

131308241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: 137995876-T-C

131308284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: synonymous variant
orthologous variants: 137995919-A-G

http://identifiers.org/hco/10/GRCh38#131308376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137996011-A-C

131308389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 137996024-G-C

http://identifiers.org/hco/10/GRCh38#131308416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137996050-A-C

131308421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996055-G-A

131308421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996055-G-T

131308436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996070-G-C

131308436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996070-G-T

131308443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996077-G-T

131308471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996090-T-C

131308507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996126-T-C

131308526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996145-A-G

131308526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996145-A-T

131308585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996206-T-G

http://identifiers.org/hco/10/GRCh38#131308730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137996352-A-C

131308731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996353-T-C

131308735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996357-G-A

131308736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996358-T-A

131309035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996638-A-T

131309090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996692-G-T

131309144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996747-C-G

131309144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996747-C-T

131309320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996936-G-A

131309333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996949-G-A

131309405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137996986-G-T

131309703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137997600-A-G

131310162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137997966-T-A

131310196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137997994-A-G

131310359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998141-T-A

131310798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998558-C-T

131310803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998563-C-T

131310903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998643-G-A

131311018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998773-T-C

http://identifiers.org/hco/10/GRCh38#131311041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137998795-C-A

131311163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998925-G-T

131311193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998955-A-G

131311193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998955-A-T

http://identifiers.org/hco/10/GRCh38#131311231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#137998980-C-A

131311231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998980-C-T

131311245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998996-G-A

131311245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: intron variant
orthologous variants: 137998996-G-T

131311538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: 137999282-G-A

131311538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: 137999282-G-C

131311538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23533
most severe consequence: missense variant
orthologous variants: 137999282-G-T