131622641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622453-C-T

131622758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622338-C-T

131622828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622269-G-A

131622828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622269-G-T

131622841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622255-T-C

131622887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622206-G-T

131622898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622195-A-G

131622938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29622157-G-C

131623218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29621900-C-T

131623322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29621797-T-C

http://identifiers.org/hco/11/GRCh38#131623553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29621566-C-A

131623744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29621391-G-A

131623786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29621346-G-A

131623786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29621346-G-T

131623893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29621239-C-T

131624318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620825-G-A

131624528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620681-T-C

131624613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620596-A-T

131624679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620530-T-C

131624778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620406-A-T

131624818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620368-G-A

131624831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620355-A-G

131624900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620285-G-T

131624972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620210-T-C

131625007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620175-C-T

131625041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620139-C-G

131625061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620119-T-C

http://identifiers.org/hco/11/GRCh38#131625149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29620035-C-A

131625155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29620030-T-A

131625555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29619697-G-C

131625574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29619636-G-T

131625760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29619455-C-T

131626018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29619257-T-A

131626059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29619219-C-T

131626060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29619218-T-A

131626928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29618431-C-T

131626930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29618429-G-T

131627006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29618353-A-G

http://identifiers.org/hco/11/GRCh38#131627196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29618153-C-A

131627198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29618151-T-A

131627198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29618151-T-C

131627253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29617384-G-A

131627253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29617384-G-C

131627345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29617296-T-C

131628684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29616514-T-C

131628770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29616447-G-A

131628775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29616442-G-T

131628818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29616396-G-A

131628959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29616260-T-G

131629034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29616158-C-T

131629116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29616088-T-C

131629205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615999-A-T

131629215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615989-C-G

http://identifiers.org/hco/11/GRCh38#131629343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29615866-C-A

131629343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615866-C-T

131629457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615751-T-C

131629459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615750-A-G

131629500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615698-C-T

131629566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615632-C-T

http://identifiers.org/hco/11/GRCh38#131629650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29615547-C-A

131629650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615547-C-T

131629798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29615399-G-A

131630370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29614823-A-T

131630666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29614282-T-C

131630878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29614079-A-G

131630982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613952-T-C

131631123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613800-T-G

131631174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613750-T-C

131631475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613187-T-C

131631495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613111-A-G

131631497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613109-G-A

131631497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613109-G-T

131631534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29613051-G-A

131631819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29612797-G-C

131633111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29612320-G-T

131633220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29612233-T-G

131633540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29611961-T-A

131633540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29611961-T-C

131634565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29611120-G-A

131634639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29611057-T-A

131634639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29611057-T-C

131636551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29610201-C-T

131636567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29610185-C-T

131636614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29610136-C-T

131636628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29610122-C-T

131636744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29610014-G-A

http://identifiers.org/hco/11/GRCh38#131636767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29609994-C-A

131636782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29609977-T-C

http://identifiers.org/hco/11/GRCh38#131636837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29609921-C-A

131637101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29609657-C-T

http://identifiers.org/hco/11/GRCh38#131637178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29609586-C-A

131637622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29609056-T-C

131637753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29608914-G-T

131637825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29608844-T-A

131637931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29608760-A-G

131637937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29608757-G-C

131638171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29608558-T-C

131638974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29606862-A-G

131639287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29606589-T-C

131639334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29606548-C-T

http://identifiers.org/hco/11/GRCh38#131639708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29606254-A-C

131639747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29606239-G-A

131640068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29606138-T-A

131640592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29605628-G-A

131640697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29605529-C-T

131640821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29605416-A-G

131640916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29605318-C-T

131641030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29605219-C-G

131641197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29604623-C-T

131641250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29604567-T-C

131641268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29604544-C-T

131642214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29603899-A-G

131642541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603574-G-C

131642600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603515-A-G

131642651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603464-A-G

131642734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603371-A-T

131642829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603275-G-A

131642829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603275-G-T

131642850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603252-C-G

131642850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603252-C-T

131642936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603166-C-T

131643047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603056-G-A

131643047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29603056-G-T

http://identifiers.org/hco/11/GRCh38#131643063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29603040-A-C

131643118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602989-C-G

131643228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602890-G-A

131643340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602800-T-C

http://identifiers.org/hco/11/GRCh38#131643378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#29602770-C-A

131643389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29602760-C-G

131643389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29602760-C-T

131643515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602625-A-G

131643653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602515-C-T

131643710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602470-G-T

131643764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602418-G-A

131643837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29602395-G-A

131644794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29601031-G-A

131645198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29600648-A-T

131645259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29600588-G-A

131645323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29600520-C-T

131645357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29600516-C-T

http://identifiers.org/hco/11/GRCh38#131645463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29600418-C-A

http://identifiers.org/hco/11/GRCh38#131645562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29600312-C-A

131645562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29600312-C-T

http://identifiers.org/hco/11/GRCh38#131645787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29600044-C-A

131645801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29600034-T-G

131645821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29600015-G-A

http://identifiers.org/hco/11/GRCh38#131646017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29599822-A-C

131646059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29599785-A-G

131646223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29599611-A-G

131646471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29598896-A-G

131646488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29598864-T-C

131646524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29598829-C-T

131647076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29598303-C-T

131647351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29598035-C-T

131647359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29598027-G-A

131647536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29597873-A-G

131647876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29597548-T-G

http://identifiers.org/hco/11/GRCh38#131648882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29596956-C-A

http://identifiers.org/hco/11/GRCh38#131649000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29596837-A-C

131649473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29596415-G-A

131649871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29596055-C-T

131649873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29596053-G-C

131649914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29596016-G-T

131649976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29595955-T-G

http://identifiers.org/hco/11/GRCh38#131650082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29595862-C-A

131650082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29595862-C-T

http://identifiers.org/hco/11/GRCh38#131650268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29595420-C-A

131650305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29595383-A-G

131650568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29594837-G-A

131650608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29594796-A-T

http://identifiers.org/hco/11/GRCh38#131650665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29594728-C-A

131650669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29594724-G-T

131650760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29594629-A-G

131650781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29594596-C-T

http://identifiers.org/hco/11/GRCh38#131650816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29594562-C-A

131650930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29594447-A-G

131650957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29594420-A-G

131651463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29593908-A-G

131651771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29593778-G-T

131652025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29593673-C-T

131652065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29593638-G-C

131652403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29593293-A-T

131652692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592995-A-G

131652922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592764-T-C

http://identifiers.org/hco/11/GRCh38#131652938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29592750-C-A

131653001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592688-C-G

131653220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592484-G-A

131653229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592475-T-C

131653353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592366-A-G

131653359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592360-G-A

131653359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592360-G-C

131653447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592277-T-A

131653650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29592054-C-T

131653721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29591991-A-G

131654143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29591640-G-A

131654493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29591330-C-T

131655225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29591106-G-A

131655225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29591106-G-C

131655486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29590854-A-G

131655722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29590601-A-G

131655911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29590418-G-A

131655929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29590400-A-G

131656105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29590253-A-T

131656163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29590198-A-G

http://identifiers.org/hco/11/GRCh38#131656381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29589999-A-C

131656381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589999-A-G

http://identifiers.org/hco/11/GRCh38#131656382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29589998-C-A

http://identifiers.org/hco/11/GRCh38#131656414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29589966-C-A

131656414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589966-C-T

131656454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589924-T-C

131656601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29589763-G-T

131656682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589685-G-A

131656682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589685-G-C

131656707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29589660-C-G

131657001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589421-G-C

131657188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589239-G-T

131657247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589185-T-C

131657373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29589044-C-T

131657682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29588731-A-G

http://identifiers.org/hco/11/GRCh38#131658165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29588077-C-A

131658238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29588005-T-G

131658351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587878-G-A

131658351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587878-G-T

131658554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587712-G-A

131658554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587712-G-C

131658554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587712-G-T

131658670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587602-G-A

131658689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587584-G-T

131659077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587501-A-T

131659165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587419-C-T

131659228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587358-G-T

131659304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587281-G-A

131659324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587264-C-T

131659446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587147-C-T

131659478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587115-G-A

131659478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587115-G-T

http://identifiers.org/hco/11/GRCh38#131659496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29587098-A-C

131659570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29587018-T-C

131659591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586995-G-A

131659747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586818-T-A

131659751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586814-G-C

131659751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586814-G-T

131659787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586782-C-G

131659787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586782-C-T

131659810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586755-T-C

131659916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586661-G-A

131659927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586650-A-G

131659945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586635-T-C

http://identifiers.org/hco/11/GRCh38#131660211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29586372-A-C

131660239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586344-C-T

131660280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586329-G-T

131660302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586307-G-A

131660302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586307-G-T

131660330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586284-G-T

131660335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586279-G-A

131660335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586279-G-T

http://identifiers.org/hco/11/GRCh38#131660340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29586274-C-A

131660340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586274-C-T

131660358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586249-A-G

131660431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586181-T-A

131660431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586181-T-C

131660557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29586051-G-A

131660677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585952-G-A

131660677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585952-G-T

http://identifiers.org/hco/11/GRCh38#131660683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29585946-A-C

131660683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585946-A-G

131660683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585946-A-T

131660709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585920-G-T

131660750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585879-G-A

131660766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585862-G-A

131660766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585862-G-T

131660947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29585680-T-A

131660947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29585680-T-C

http://identifiers.org/hco/11/GRCh38#131660999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#29585627-C-A

131660999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29585627-C-T

131661084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585539-A-G

131661137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585489-G-A

131661137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585489-G-C

131661137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585489-G-T

131661220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585414-A-T

131661264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585369-A-G

http://identifiers.org/hco/11/GRCh38#131661266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29585367-A-C

131661266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585367-A-G

http://identifiers.org/hco/11/GRCh38#131661311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29585323-C-A

131661311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585323-C-T

131661319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585315-A-G

131661319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585315-A-T

http://identifiers.org/hco/11/GRCh38#131661324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29585310-C-A

131661325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585309-T-A

131661325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585309-T-C

131661325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585309-T-G

http://identifiers.org/hco/11/GRCh38#131661332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29585301-A-C

131661332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585301-A-G

131661332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585301-A-T

131661334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585299-T-A

131661334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585299-T-C

131661334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585299-T-G

131661603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29585030-G-A

131661668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29584966-T-C

131661836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29584812-A-T

131662197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29584445-T-C

131662200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29584442-T-A

131662328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29584324-T-C

http://identifiers.org/hco/11/GRCh38#131662416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29584237-C-A

131662416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 29584237-C-T

http://identifiers.org/hco/11/GRCh38#131662419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29584234-C-A

131662439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29584214-T-C

131662718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29583973-G-T

131662827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29583868-C-T

131662838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29583857-C-T

131662951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29583746-G-A

131663084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29583618-G-C

131663084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29583618-G-T

http://identifiers.org/hco/11/GRCh38#131663221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29583504-C-A

http://identifiers.org/hco/11/GRCh38#131663235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29583490-C-A

131663235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29583490-C-G

http://identifiers.org/hco/11/GRCh38#131663299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#29583429-C-A

131663299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29583429-C-T

131663478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29583257-G-A

131663478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29583257-G-T

131663487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29583239-G-T

131663598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29583125-C-T