71188115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23537553-G-T

71188612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536853-G-A

71188672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536808-T-C

71188759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536780-C-T

71189081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536561-T-A

71189081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536561-T-C

71189097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536545-T-A

http://identifiers.org/hco/6/GRCh38#71189131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23536513-C-A

71189353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536248-C-G

71189430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23536169-A-G

71189670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23535951-A-G

71196318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23533959-G-C

http://identifiers.org/hco/6/GRCh38#71196659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23533680-A-C

71196659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23533680-A-T

71197147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23533235-A-G

71197169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23533223-T-C

71197170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23533222-A-G

71197350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23533054-C-G

71197350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23533054-C-T

71197497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23532909-C-T

71197679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23532743-T-A

71197752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23532694-C-T

71197905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23532595-T-C

71198009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23532496-A-G

71198069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23532431-T-C

71198231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23532287-C-T

71198264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23532254-A-T

71198559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531428-G-A

71198559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531428-G-T

71198571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531422-G-A

71198664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531346-A-G

71198894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531123-C-T

71198904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531113-G-A

71198904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531113-G-C

71198904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23531113-G-T

71199122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23530897-G-A

71199122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23530897-G-T

71199218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23530737-T-C

71199296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23530659-C-T

71199550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23530277-C-T

71199632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23530225-A-G

71199647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23530218-T-C

71200061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23529813-C-T

71200068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23529806-C-T

71200426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23529406-G-A

71200426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23529406-G-T

http://identifiers.org/hco/6/GRCh38#71201233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23529051-A-C

71201233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23529051-A-G

71201370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528871-G-T

71201493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528747-T-C

71201515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528725-A-G

71201515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528725-A-T

71201719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528539-T-C

http://identifiers.org/hco/6/GRCh38#71201767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23528497-C-A

71201767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528497-C-T

71201824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528466-T-C

71201970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528367-C-T

71202017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528339-T-A

71202070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23528294-C-G

71204450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527340-T-G

71204498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527318-A-G

71204527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527291-C-T

71204560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527261-T-C

71204668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527152-T-C

71204672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527148-C-T

71204685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527135-A-G

71204750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23527061-C-T

71204851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23526964-G-A

71204851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23526964-G-C

71204975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23526846-A-G

71205035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23526791-G-C

71205220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23526609-G-A

71205220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23526609-G-C

71209293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23520591-C-G

71209349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23520543-A-G

http://identifiers.org/hco/6/GRCh38#71209588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23520327-C-A

71209922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23519988-A-G

71210138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23515311-T-G

71210373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23515064-T-C

71210385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23515051-G-A

http://identifiers.org/hco/6/GRCh38#71210472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23514845-C-A

71210550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23514790-C-T

71210777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23514479-A-G

71210947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23514291-T-C

71210986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23514257-C-T

71210993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23514250-A-G

71216337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23513531-G-A

71216457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23513407-G-A

71216457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23513407-G-T

71216759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23513128-C-G

71216759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23513128-C-T

71216840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23513031-T-C

71216868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23513006-A-G

71217174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23512735-A-G

71217363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23512567-A-G

71217553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23512408-T-G

71217759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23512223-C-T

71218020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23511962-T-C

71218340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23511662-A-G

71220213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23507609-T-C

71220238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23507580-C-T

71220387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23507440-C-T

71220679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23507170-C-T

71222803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23506609-T-C

71222870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23506546-A-G

71223066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23506401-C-T

71223145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23506327-T-C

71223226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23506241-T-A

71223246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23506222-A-T

http://identifiers.org/hco/6/GRCh38#71223358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23506099-A-C

71223471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23505964-T-C

71223579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23505859-A-T

71223630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23505808-A-G

71224347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23505488-C-G

http://identifiers.org/hco/6/GRCh38#71224504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23505344-C-A

71224504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23505344-C-G

71224530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23505318-G-C

71224559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23505286-T-C

71224719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23505137-T-C

71225120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23504890-T-C

71225844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23503838-T-C

71225978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23503713-G-T

71225980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23503711-A-G

71225998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23503697-T-C

http://identifiers.org/hco/6/GRCh38#71226135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23503568-C-A

71226135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23503568-C-T

71226149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23503554-G-A

71226149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23503554-G-T

71226335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23503369-C-T

71226836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23502865-T-C

71226854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23502847-T-C

http://identifiers.org/hco/6/GRCh38#71227503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23501970-C-A

71227843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23501739-C-G

http://identifiers.org/hco/6/GRCh38#71228179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23501408-C-A

71228179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23501408-C-T

71228294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23501157-G-T

71228300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23501151-A-T

71228478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23500990-C-T

71228784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23500621-A-G

71228965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23500469-A-G

71229160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23500069-A-G

71229374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23499856-T-C

71229374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23499856-T-G

71229423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23499815-A-G

71229437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23499801-C-T

71229605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23499652-T-C

71233415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23492815-A-G

71233559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non coding transcript exon variant
orthologous variants: 23492640-G-T

71233637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non coding transcript exon variant
orthologous variants: 23492591-T-C

71237365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23488183-G-C

71237580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23487966-C-T

71237585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23487961-T-C

http://identifiers.org/hco/6/GRCh38#71238132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23487339-A-C

71238301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23487220-C-T

71238302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23487219-A-T

71238475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23487031-G-A

71238487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23487019-G-A

71238515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23486991-G-A

71238515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23486991-G-T

71238651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23486856-T-A

71238750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23486772-G-T

71238793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23486263-C-T

71238827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23486229-G-A

71238928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23486127-T-A

71246758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23485075-C-T

71246858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484962-C-T

71246869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484951-C-T

71246925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484905-T-C

71246961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484863-T-C

71246964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484860-T-C

http://identifiers.org/hco/6/GRCh38#71247038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23484785-C-A

71247058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484766-T-G

71247185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484650-T-C

71247342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484506-C-T

71247403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484442-C-T

71247683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484173-T-G

71247731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484123-T-C

71247918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483949-G-T

http://identifiers.org/hco/6/GRCh38#71248171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23483689-C-A

71248381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23483509-A-G

71248381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23483509-A-T

71248472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23483429-A-G

71248733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23483178-C-T

71248757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23483150-C-G

71248757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23483150-C-T

71249105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23482774-T-G

71250157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473245-G-A

71250217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473203-A-G

71250253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473167-C-T

71250270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473151-T-C

71250460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23472963-C-T

71250463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23472960-A-T

71250509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472913-G-C

71250626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472786-A-G

http://identifiers.org/hco/6/GRCh38#71251939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23471628-A-C

71251986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471589-A-G

71252031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471549-T-C

http://identifiers.org/hco/6/GRCh38#71252132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23471444-A-C

71252132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471444-A-G

71252133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471443-A-G

71252133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471443-A-T

71252135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471441-T-C

71252329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471319-G-C

71252479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471212-A-G

71252479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471212-A-T

71252619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471114-A-G

71252641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471098-G-T

71252645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471094-G-A

71252645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471094-G-T

71252648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23471091-A-G

http://identifiers.org/hco/6/GRCh38#71252717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23471035-A-C

71252773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23470998-G-A

71252835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23470950-G-C

71252835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23470950-G-T

71255589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461888-T-C

71255666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461653-C-T

71256619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461353-G-A

71256661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461310-A-G

71256700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461286-A-G

71256710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461276-G-A

71256710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461276-G-T

71256794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461222-T-A

71256825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461190-T-A

71257137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460890-C-T

71257208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460829-T-A

71257220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460817-G-A

71257220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460817-G-T

71257307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460725-G-A

71257396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460594-G-T

71257412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460514-G-C

71257478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460453-G-T

71257517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460414-T-C

71257575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460338-G-C

71257583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460330-T-C

71257697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460212-G-A

71257924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460002-C-T

71257948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459984-C-G

71258208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459725-A-G

71258480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459508-G-C

71258480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459508-G-T

71258502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459486-G-A

71258571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23458267-T-A

71258668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458170-A-T

71258766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458067-T-G

71258827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458004-A-G

71258828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458003-G-C

71258851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23457980-T-C

71258855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23457976-G-C

71258884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23457971-G-A

71258909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23457947-G-T

71258914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23457942-G-A

71259090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23457772-A-G

71259775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23456906-G-A

http://identifiers.org/hco/6/GRCh38#71259942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23456722-A-C

71259942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23456722-A-G

http://identifiers.org/hco/6/GRCh38#71260107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23456563-C-A

71260107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23456563-C-G

http://identifiers.org/hco/6/GRCh38#71260312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23456363-A-C

71260331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23456346-G-A

71260487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23455714-T-C

71260712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23455491-G-T

71260840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23455382-A-G

71261039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23454808-A-G

71261118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23454731-T-C

71261188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23454658-T-C

71261337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23454510-C-T

71261618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23454261-G-A

71261819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23454078-G-A

71261839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23454035-A-G

71262024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23453666-C-T

71262330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23453434-T-A

71262711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23451383-C-T

71262976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450991-C-T

71263322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450565-T-A

71263423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450411-A-T

http://identifiers.org/hco/6/GRCh38#71263505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23450336-C-A

71263505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450336-C-T

71263590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450252-A-T

71263832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450028-G-A

71263842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450018-G-A

http://identifiers.org/hco/6/GRCh38#71263968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23449631-C-A

71264038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23449564-T-C

71264195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23449399-T-C

http://identifiers.org/hco/6/GRCh38#71264229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23449361-A-C

71264380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23449221-T-C

http://identifiers.org/hco/6/GRCh38#71264462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23449151-A-C

71264536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23449085-A-G

71265234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23448488-A-G

71265346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23448410-T-C

71269420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23441274-T-G

71269488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23441210-G-A

71269490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23441208-G-T

http://identifiers.org/hco/6/GRCh38#71279244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23432202-A-C

http://identifiers.org/hco/6/GRCh38#71279593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23431991-A-C

71279864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431694-T-C

71280193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431348-C-T

71280296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431279-T-G

71280297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431278-T-G

71280302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431273-G-C

71280303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431272-T-A

71280312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431263-T-C

71280337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431241-A-T

71280401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431186-A-G

71280486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431101-C-T

71280575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431016-T-C

71280606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23430984-T-G

71280896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23430728-C-G

71280902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23430722-G-T

http://identifiers.org/hco/6/GRCh38#71281496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23430113-C-A

71281496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23430113-C-T

71281510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23430099-G-T

71281686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429962-T-A

71281686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429962-T-C

71281736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429905-G-A

71281736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429905-G-C

http://identifiers.org/hco/6/GRCh38#71281769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23429873-C-A

71281769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429873-C-T

71282120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429538-T-A

71282193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429466-G-C

71282210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429449-G-A

71282237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429435-T-C

71282409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429147-C-T

71282420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23429136-T-A

71282467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23428918-G-A

71282474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23428911-A-G

71282538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23428779-T-A

71282676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23428651-A-G

http://identifiers.org/hco/6/GRCh38#71282833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23428548-A-C

71282996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23428363-T-A

71283231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23428126-T-C

71283262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23428095-G-T

71283404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23427984-C-T

71283505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23427875-A-G

71284018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23427421-G-A

71284018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23427421-G-T

71284107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23427331-C-G

71284515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23427227-T-A

71284635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23427117-C-G

71284857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426928-T-C

71284932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23426852-T-C

http://identifiers.org/hco/6/GRCh38#71284934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23426850-C-A

71285026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23426776-C-T

71285097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426714-G-T

71285171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426686-T-G

71285328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426539-A-G

71285558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426325-T-C

71285878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425239-C-T

71286102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425017-T-C

71286273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424856-T-G

71286291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424851-G-A

71286351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424802-G-A

71286593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424582-G-A

71288129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422834-A-G

71288662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422370-G-A

71288662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422370-G-T

71288670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422362-G-A

71288670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422362-G-T

71288687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422349-G-A

71288687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422349-G-T

71288716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422333-G-A

71288716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422333-G-T

71288725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422324-G-A

71288725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422324-G-C

71288725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422324-G-T

http://identifiers.org/hco/6/GRCh38#71288772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23422277-C-A

http://identifiers.org/hco/6/GRCh38#71288784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23422265-C-A

71288784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422265-C-T

71288811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422234-A-G

71288811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422234-A-T

71289015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422052-T-A

71289015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422052-T-C

71289015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422052-T-G

http://identifiers.org/hco/6/GRCh38#71289021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23422046-C-A

71289021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23422046-C-T

71289215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421845-A-G

71289215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421845-A-T

http://identifiers.org/hco/6/GRCh38#71289221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23421839-C-A

71289221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421839-C-T

http://identifiers.org/hco/6/GRCh38#71289284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23421789-C-A

71289284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421789-C-T

http://identifiers.org/hco/6/GRCh38#71289296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23421777-A-C

71289296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421777-A-G

71289385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23421731-G-T

http://identifiers.org/hco/6/GRCh38#71289400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23421716-C-A

71289400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23421716-C-T

71289413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23421703-T-A

http://identifiers.org/hco/6/GRCh38#71289423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23421692-C-A

71289432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23421683-A-G

71289432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23421683-A-T

71289933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421180-G-C

71290270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420945-C-G

71290300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420915-C-G

71290329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420890-T-A

71290731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420527-A-G

71290734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420524-G-A

71291138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420107-A-G

71291158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420088-T-C

71291158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420088-T-G

71291311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419944-G-C

71291311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419944-G-T

http://identifiers.org/hco/6/GRCh38#71291316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23419939-C-A

71291316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419939-C-G

71291316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419939-C-T

71291441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419872-T-C

71291462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419852-G-A

71291473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419841-T-C

71291487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419834-G-A

71291500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419821-A-G

71291557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419756-G-A

71291557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419756-G-T

71291593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419726-G-A

71291593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419726-G-T

71291598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419721-A-G

71291625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419700-A-G

71291628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419697-A-G

http://identifiers.org/hco/6/GRCh38#71291665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23419669-C-A

71291665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419669-C-T

71291772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419562-C-T

71291790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419544-G-A

71291790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419544-G-T

71291797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419537-T-A

71291798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419533-T-C

71291809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419522-T-C

http://identifiers.org/hco/6/GRCh38#71291898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23419423-C-A

71291948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23419384-G-T

71291972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23419359-C-T

71291977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23419354-A-T

71292094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419299-T-A

71292361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419045-G-A

71292754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418651-G-A

71293141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418280-T-C

71293239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418182-T-C

71293272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418158-G-C

71293338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23418092-T-C

71293385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418045-A-G

http://identifiers.org/hco/6/GRCh38#71293464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23417986-C-A

71293464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417986-C-T

71293480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417970-A-G

http://identifiers.org/hco/6/GRCh38#71293605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23417811-C-A

http://identifiers.org/hco/6/GRCh38#71293715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23417674-C-A

71293715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417674-C-G

71293715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417674-C-T

71293723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417666-T-C

71293768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417588-T-C

http://identifiers.org/hco/6/GRCh38#71293829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23417470-A-C

71293948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417354-G-A

71293989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417279-T-C

71294047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417222-T-A

71294257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417072-A-G

71294306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417017-A-G

http://identifiers.org/hco/6/GRCh38#71294392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23416939-C-A

71294533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23416828-T-C

71295257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23416180-T-C

71296174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415464-T-C

http://identifiers.org/hco/6/GRCh38#71296241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23415410-C-A

71296242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415409-T-C

71296322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23415323-T-C

71296405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415240-A-G

71296412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415233-C-G

71296483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415143-T-A

http://identifiers.org/hco/6/GRCh38#71296502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23415126-C-A

71296651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414977-T-G

71296857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414742-T-C

71296876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414724-G-A

71296876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414724-G-C

71297062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414279-C-G

http://identifiers.org/hco/6/GRCh38#71297082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23414264-A-C

71297100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414246-C-T

71297319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414051-T-G

71297422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413954-T-A

71297687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413726-C-T

71298066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413620-C-T

71298125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413566-C-T

71298618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413133-T-C

71298792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412677-A-G

71299134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412359-T-C

71299273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412245-A-G

71299341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412180-A-G

71299532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411974-G-A

http://identifiers.org/hco/6/GRCh38#71299675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23411869-C-A

71299689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411855-A-G

71300112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411324-G-A

71300636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23410716-T-C

71300764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23410512-A-G

71301103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409800-A-G

71301277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409633-T-C

71301315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409598-C-T

71301333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409580-T-C

71301537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23409376-T-C

71301682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23409231-C-T

71301831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23409082-C-T

71301890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23409023-T-A

71301890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23409023-T-C

http://identifiers.org/hco/6/GRCh38#71301935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23408978-C-A

71302236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408654-T-A

71302236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408654-T-C

http://identifiers.org/hco/6/GRCh38#71302904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23408369-C-A

71302917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408356-A-G

http://identifiers.org/hco/6/GRCh38#71302970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23408310-C-A

71303320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408268-A-G

71303378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408208-G-T

71303379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408207-T-C

71303396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408190-G-T

71303566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23408002-G-T

71303829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23407608-T-C

71304118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23407280-T-G

71304119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23407279-T-C

71304187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23407199-A-T

71304263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23407127-G-A

http://identifiers.org/hco/6/GRCh38#71304367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23407026-C-A

71304367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23407026-C-G

71304372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23407021-T-C

http://identifiers.org/hco/6/GRCh38#71304649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23406515-C-A

71304656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23406508-A-G

http://identifiers.org/hco/6/GRCh38#71304742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23406423-C-A

71304742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23406423-C-T

http://identifiers.org/hco/6/GRCh38#71304840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23406325-C-A

71305038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23406125-T-C

71305099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23406064-A-G

71305185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405975-T-C

71305248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405919-C-T

71305310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405849-T-C

71305326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405833-G-T

http://identifiers.org/hco/6/GRCh38#71305384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23405783-C-A

71305390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405777-T-C

71305426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405741-G-A

71305563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405610-T-G

71305569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405604-A-T

71305574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405599-G-T

71305689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405500-C-G

71305804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405395-A-G

71305858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405349-G-T

http://identifiers.org/hco/6/GRCh38#71306109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23405153-C-A

71306140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405120-G-A

71306140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405120-G-T

71306177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405078-A-G

71306203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405052-A-G

71306263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405003-G-T

71306342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23404929-T-C

http://identifiers.org/hco/6/GRCh38#71306394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23404880-C-A

71306394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23404880-C-G

71306864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23403713-G-T

http://identifiers.org/hco/6/GRCh38#71307330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23403285-C-A

71307330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23403285-C-T

71307955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23401068-G-T

71308030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23400993-G-T

71308226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23400845-T-G

71308430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23400384-C-T

http://identifiers.org/hco/6/GRCh38#71308571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#23400255-C-A

71308784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23400056-A-G

71308903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23399930-T-C

71309196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399644-A-T

71309226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399616-C-T

71310403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23397870-G-A

71310403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23397870-G-T

71310406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23397867-A-G

71310555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23397754-T-C

71310588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23397729-A-G

http://identifiers.org/hco/6/GRCh38#71310612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23397705-C-A

71310625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23397691-A-G

http://identifiers.org/hco/6/GRCh38#71310945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23397403-C-A

71310945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23397403-C-T

71311050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397344-T-A

71311239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397170-A-T

71311409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397027-G-A

71312620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395755-A-T

71312984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394747-C-T

71313065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23394666-C-T

71313202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23394536-C-G

71313268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23394459-T-C

71313269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23394458-T-C

71313394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23394319-C-T

http://identifiers.org/hco/6/GRCh38#71313543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23394145-A-C

71313543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23394145-A-T

71313653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23394030-G-A

http://identifiers.org/hco/6/GRCh38#71314054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23393684-C-A

71314071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393667-G-A

71314083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393664-T-C

71314100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393647-A-G

71314308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393438-A-G

71314309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393437-G-A

71314505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393245-T-G

http://identifiers.org/hco/6/GRCh38#71314560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23393190-A-C

http://identifiers.org/hco/6/GRCh38#71314681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23393085-C-A

71314681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393085-C-T

71314704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23393063-T-C

71314872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23392892-C-T

http://identifiers.org/hco/6/GRCh38#71315104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23392666-C-A

71315111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23392659-G-C

71315161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23392609-T-C

71315186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23392591-T-C

71315241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23392539-T-C

71319707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23385801-G-A

http://identifiers.org/hco/6/GRCh38#71319817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23385879-C-A

71319817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23385879-C-T

71320057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386290-T-C

71320109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386339-C-T

71320331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386557-T-C

71320485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386705-C-G

71320485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386705-C-T

71320545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386765-G-C

71320637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386848-G-A

71321054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387197-G-A

71321187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387341-T-A

71321188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387342-G-T

71321264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387416-G-A

71321305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387462-A-G

71321997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388107-T-C

71322178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388343-T-C

http://identifiers.org/hco/6/GRCh38#71322260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23388494-C-A

71322260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388494-C-T

71322309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388588-G-A

71322379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388679-G-A

71322549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388843-G-C

71322583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388877-A-G

71322605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388899-G-A

71322709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388969-T-A

71322932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389187-A-T

http://identifiers.org/hco/6/GRCh38#71323016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23389272-C-A

http://identifiers.org/hco/6/GRCh38#71323032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23389288-A-C

71323335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389566-G-A

71323477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389697-T-C

71324019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390210-G-C

71330881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23383410-A-G

http://identifiers.org/hco/6/GRCh38#71330952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23383344-A-C

71331016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23383296-G-A

71331784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23382759-C-T

http://identifiers.org/hco/6/GRCh38#71332050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23382553-C-A

71332078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23382526-C-T

http://identifiers.org/hco/6/GRCh38#71332118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23382486-C-A

71332158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23382448-C-T

71332255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23382352-G-A

71332462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23382128-G-A

71332720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23381875-G-A

http://identifiers.org/hco/6/GRCh38#71333148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23381445-C-A

71333613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380974-T-C

71333618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380969-T-C

71333649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380938-G-A

71333783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380798-G-A

71333783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380798-G-T

http://identifiers.org/hco/6/GRCh38#71333851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23380731-C-A

71333851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380731-C-T

71334311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380534-G-C

http://identifiers.org/hco/6/GRCh38#71334318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23380527-C-A

71334318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380527-C-G

71334331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380517-T-G

71334597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380266-C-T

71334784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380148-C-T

http://identifiers.org/hco/6/GRCh38#71334841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23380092-A-C

71334848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23380085-G-A

71338225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376638-T-C

71338490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376399-G-A

71338551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376336-T-A

71338551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376336-T-C

71338820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376072-A-T

71338846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376046-T-G

71338864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376026-C-T

71338912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375990-A-G

71339426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375472-T-C

71339497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375408-G-A

71339868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374719-T-G

71339887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374700-T-C

71339897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374690-T-G

71340230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374377-C-T

http://identifiers.org/hco/6/GRCh38#71340239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23374368-A-C

71340368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374242-A-G

71340425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374185-G-T

71340426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374184-C-T

71340763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374024-G-A

71340871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373903-A-G

71340895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373879-G-A

71340895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373879-G-T

71341156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373651-T-C

http://identifiers.org/hco/6/GRCh38#71341199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23373601-A-C

71341206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373594-C-T

71341665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373121-C-T

71342082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23372478-G-T

71342244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23372310-A-T

71342766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371812-C-T

71343067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371514-G-A

71343067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371514-G-T

http://identifiers.org/hco/6/GRCh38#71343185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23371401-C-A

71343258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371330-C-G

71343297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371319-T-C

http://identifiers.org/hco/6/GRCh38#71343436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23371184-A-C

71343436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371184-A-T

71343593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371050-C-G

71343950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370720-A-G

71343972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370698-G-T

71344065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370612-C-T

71344139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370574-T-C

71344179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370533-T-C

71344210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370508-A-G

71344228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370490-T-C

71344261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370471-G-T

71344284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370449-T-C

71344284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370449-T-G

71344293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370440-G-A

71344293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370440-G-T

71344297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370436-G-T

71344314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370423-G-C

71344356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370392-T-A

http://identifiers.org/hco/6/GRCh38#71344358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23370390-C-A

71344358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23370390-C-T

71344666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23369398-G-A

http://identifiers.org/hco/6/GRCh38#71344682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23369382-C-A

http://identifiers.org/hco/6/GRCh38#71344714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23369350-C-A

71344746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369320-A-T

71344800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369279-G-A

71344824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369255-G-A

71344828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369248-A-G

71344841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369235-G-T

71344848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369228-T-C

71344869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369209-G-A

71344888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369190-C-T

71345077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369010-T-A

71345077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369010-T-C

http://identifiers.org/hco/6/GRCh38#71345101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23368981-C-A

71345133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368951-C-T

71345248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368851-C-T

http://identifiers.org/hco/6/GRCh38#71345302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23368797-A-C

71345349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368740-G-A

71345539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368510-T-C

71345693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368363-G-C

71345802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368258-C-T

71345895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368148-T-C

71345936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368081-C-T

71346031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367819-T-C

71346050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367799-G-A

71346067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367779-A-G

71346273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367604-T-C

71346319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367560-C-T

71346328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367551-T-C

71346415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367462-C-T

71346421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367456-T-C

71346648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367204-T-C

71346722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367129-T-C

71346773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367080-A-G

71346809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23367063-A-G

71346902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366329-G-T

71347041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366208-G-A

71347126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366139-T-C

71347130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366135-T-A

71347130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366135-T-C

71347283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366000-G-C

http://identifiers.org/hco/6/GRCh38#71347312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23365977-C-A

71347468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365833-T-A

71347501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365802-C-T

71347729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365587-C-G

71347793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365524-T-C

71348017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365342-T-C

71348561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23365160-T-C

71348793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23364942-A-G

71349304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363824-A-G

71349766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23361832-A-G

71350189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23361071-A-T

71350399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360857-A-T

71350826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360437-A-G

71351029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360263-T-C

71351529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358699-T-A

71351529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358699-T-C

71351710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358530-A-T

71351732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358455-A-T

71352423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357853-T-C

71352966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357651-A-G

http://identifiers.org/hco/6/GRCh38#71353034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23357581-A-C

71353034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357581-A-T

71353124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357501-A-G

71353278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357387-T-C

71353342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357332-T-A

71354049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23356618-T-C

http://identifiers.org/hco/6/GRCh38#71354060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23356606-C-A

71354441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23356349-T-C

71354503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23356280-T-C

71354754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23355617-T-C

71355068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354034-C-T

71355138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353971-T-C

71355209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353906-T-A

71369464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23334790-C-T

71369479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23334775-T-C

http://identifiers.org/hco/6/GRCh38#71370027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23334059-A-C

71370031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23334056-G-A

71375138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23332585-A-G

71375551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23332258-T-A

71375551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23332258-T-G

71376013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23331818-C-T

71376837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330967-G-A

71376837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330967-G-T

71376915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330894-A-G

71377077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330742-G-A

71377139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330677-G-T

71377542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330319-T-C

71378035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23329873-T-C

71378072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23329842-T-C

71378116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23329793-G-C

71379181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23329541-C-T

71379896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23328972-G-A

http://identifiers.org/hco/6/GRCh38#71380690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23328256-A-C

71380871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23328113-G-A

71381251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327777-T-C

71381543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327518-G-C

http://identifiers.org/hco/6/GRCh38#71381558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23327513-A-C

71382489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327331-T-C

71382881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23326974-G-A

71382883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23326972-T-C

http://identifiers.org/hco/6/GRCh38#71383280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23326680-C-A

71383280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23326680-C-G

71383317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23326649-T-C

71383390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23326614-C-T

71383600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23326480-A-G

71384102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326051-C-T

71384119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326038-A-T

http://identifiers.org/hco/6/GRCh38#71384123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23326034-A-C

71384124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326033-A-G

71384147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326012-C-T

71384264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325912-T-C

71385096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325242-T-C

71385169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325167-T-C

71386474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324471-G-A

http://identifiers.org/hco/6/GRCh38#71386739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23324217-C-A

71387433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23323619-G-A

71387502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23323558-G-A

71387502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23323558-G-T

71388206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23322941-G-A

71388206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23322941-G-T

71388319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23322851-T-C

71388431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23322757-A-G

71388554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23322618-G-T

71388577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23322595-G-C

71388617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23322551-T-C

71388704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23322469-G-T

71389097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23322107-C-T

71389293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321935-G-T

71389322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321906-G-A

71389322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321906-G-T

http://identifiers.org/hco/6/GRCh38#71389323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23321905-C-A

71389333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321895-T-A

71389341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321887-T-C

http://identifiers.org/hco/6/GRCh38#71389384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23321852-C-A

71389384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321852-C-T

71389391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321847-G-A

71389391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321847-G-C

71389391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321847-G-T

http://identifiers.org/hco/6/GRCh38#71389455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23321778-C-A

http://identifiers.org/hco/6/GRCh38#71389546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23321694-C-A

71390660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320610-T-A

71390660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320610-T-C

71390660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320610-T-G

71390661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320609-G-T

71390923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320484-G-T

71391592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320020-T-C

71392959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23319741-T-C

71393131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23319580-G-C

71393223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23319498-G-A

71393668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23319057-T-C

71393763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23318964-T-G

http://identifiers.org/hco/6/GRCh38#71393826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23318905-A-C

71394503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23318290-A-G

71394503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23318290-A-T

71394576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23318224-A-T

71394744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317662-A-G

http://identifiers.org/hco/6/GRCh38#71395196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23317238-C-A

71395266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317187-C-T

http://identifiers.org/hco/6/GRCh38#71395389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23317088-A-C

71395404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317066-G-T

71395515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316899-G-A

71395515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316899-G-T

http://identifiers.org/hco/6/GRCh38#71395786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23316655-C-A

71396038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316412-C-T

http://identifiers.org/hco/6/GRCh38#71396201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23316247-C-A

71396249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316217-A-T

71396285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316180-T-C

71396351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316117-T-C

71396393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316069-T-C

71397174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315432-T-C

71397398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315213-C-T

71397474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315198-T-G

71397909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314818-A-G

71399738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314678-C-G

71400009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314509-T-C

71400071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314445-A-G

71400148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314368-T-C

71400769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313654-T-C

71400772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313651-G-A

71400797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313626-C-T

http://identifiers.org/hco/6/GRCh38#71401094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23313359-A-C

71401319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313134-A-T

71402082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312664-G-C

71402082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312664-G-T

71403098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311843-T-G

71403120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311812-A-G

71403176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311754-T-G

71403631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311338-A-G

71403685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311287-A-G

71403708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311264-G-A

71403708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311264-G-T

71403942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311060-T-C

71404009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311003-G-A

71404265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310779-T-G

71404750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23310295-T-C

71404750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23310295-T-G

71405722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23309384-G-A

71406022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23309102-C-T

71406037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23309087-C-G

71406060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23309065-T-C

71406311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23308780-C-T

71406464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23308637-G-A

71406687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23308397-A-G

71406875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23308198-C-T

71407475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23307530-T-A

71407623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23307396-C-T

71408057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306851-T-C

71408079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306814-G-A

71408190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306628-T-C

71409588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23305397-A-G

71410593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23305074-C-G

71410671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23305003-A-G

71410865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23304826-A-T

71411880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23303828-T-C

http://identifiers.org/hco/6/GRCh38#71411917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23303791-A-C

71412498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23303239-T-C

71412519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23303218-G-C

71413076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23302735-G-A

71413281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23302582-A-G

71413485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23302416-T-C

71413544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23302350-T-C

71414098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23301518-A-T

71414439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23301157-T-C

71414664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23300954-G-A

71414842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23300775-C-T

http://identifiers.org/hco/6/GRCh38#71415273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23299912-C-A

71415273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23299912-C-T

http://identifiers.org/hco/6/GRCh38#71415442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23299807-C-A

71415983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23299418-G-C

http://identifiers.org/hco/6/GRCh38#71416143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23299263-C-A

71416397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23298988-T-C

71416433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non coding transcript exon variant
orthologous variants: 23298960-A-T

http://identifiers.org/hco/6/GRCh38#71416983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23298417-C-A

71416983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23298417-C-T

http://identifiers.org/hco/6/GRCh38#71417527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23298044-C-A

71417750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297970-A-G

71417845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297875-A-G

71418186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297656-T-A

71418186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297656-T-C

71418287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297552-T-A

71418597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297259-C-G

71418617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297239-G-T

71418625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297231-A-T

71418806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297051-A-G

71418975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296892-G-A

71418975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296892-G-C

71419352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296518-C-T

71419710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296140-G-A

71419786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296073-C-G

71419823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296036-C-G

http://identifiers.org/hco/6/GRCh38#71419924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23295942-C-A

71419924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295942-C-T

http://identifiers.org/hco/6/GRCh38#71420041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#23295852-C-A

71420041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295852-C-T

71420262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non coding transcript exon variant
orthologous variants: 23295727-G-A

71420521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non coding transcript exon variant
orthologous variants: 23295569-T-C

71420673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non coding transcript exon variant
orthologous variants: 23295474-G-T

71420724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 23295456-G-C

71420724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21380
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 23295456-G-T