203090733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 134212769-G-A

203090781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212728-G-T

203090800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212709-G-A

203090800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212709-G-T

203090849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212680-G-C

203091126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212459-G-A

203091126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212459-G-T

203091349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212233-A-G

203091372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212223-T-G

203091403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212193-G-A

203091428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212171-T-A

http://identifiers.org/hco/1/GRCh38#203091567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134212035-C-A

203091567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212035-C-T

203091584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212023-G-A

203091591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134212016-T-C

203091650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134211274-T-C

203091657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134211267-A-G

203091970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134211042-T-C

203092093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134210936-T-C

203092136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134210894-G-A

http://identifiers.org/hco/1/GRCh38#203092832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134210350-C-A

203093187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134210046-C-T

203098306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134205724-G-A

203098755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134205246-C-T

203098869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134205171-A-G

203098994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134205051-C-G

203099400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134204669-C-T

203099617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134204404-C-T

203099620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134204401-T-C

203099642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134204379-T-G

http://identifiers.org/hco/1/GRCh38#203100132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134203940-C-A

203100260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134203851-G-A

203100332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134203811-C-T

203100450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134203755-A-T

http://identifiers.org/hco/1/GRCh38#203100657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134203617-C-A

http://identifiers.org/hco/1/GRCh38#203101742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134203054-C-A

203101914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134202898-G-A

203102277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134202559-G-T

203102429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134202413-G-A

203102429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134202413-G-T

203102657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134202197-G-T

203102724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134202135-G-A

203102872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134202001-C-T

http://identifiers.org/hco/1/GRCh38#203102955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134201925-A-C

203103080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201802-A-T

203103501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201411-T-C

203103514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201398-T-C

203103579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201329-G-A

203103582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201327-G-C

203103704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201193-G-A

203103704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201193-G-T

203103714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134201183-G-A

203103850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134200897-A-T

203104015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134200739-C-T

203104042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134200720-C-G

203104042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134200720-C-T

203104369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134200426-A-G

203114481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134176926-C-T

203114844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134176146-T-C

203115995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134173545-T-C

http://identifiers.org/hco/1/GRCh38#203116212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#134173343-C-A

203116239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134173316-G-A

http://identifiers.org/hco/1/GRCh38#203116514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134173061-C-A

203116534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134173041-G-T

203116560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134173015-G-C

203116718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172883-C-T

203117283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172475-C-G

203117283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172475-C-T

203117293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172465-C-T

203117295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172463-C-T

203117587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172348-T-G

203117610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172325-A-G

203117804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134172208-G-A

203118133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134172024-T-C

203118350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171867-G-A

203118513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171669-C-T

203118618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171589-C-T

203118850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171401-G-A

203119060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171222-G-A

203119060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171222-G-C

203119839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134170580-A-G

203119893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134170527-A-G

203119894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134170526-G-A

203120297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134170021-C-T

203120350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169953-C-T

203120372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169937-G-A

203120828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169494-C-T

http://identifiers.org/hco/1/GRCh38#203120864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134169465-A-C

203120864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169465-A-G

203120864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169465-A-T

203121197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169114-A-G

203121240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169070-C-T

203121269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134169038-C-G

http://identifiers.org/hco/1/GRCh38#203121678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134168675-C-A

203121678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168675-C-T

203122134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168193-G-T

203122234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168142-T-A

203123344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167531-G-A

203123344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167531-G-C

203123369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167510-A-G

203123432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167451-C-T

203123512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167394-C-G

http://identifiers.org/hco/1/GRCh38#203123544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134167369-C-A

203123544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167369-C-T

203123546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167366-C-T

203123558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167354-G-A

203123559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167353-C-T

203123617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167299-T-G

203123700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167207-T-C

203123762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167131-G-A

http://identifiers.org/hco/1/GRCh38#203123772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134167121-C-A

203123856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166971-C-T

203123979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166856-G-T

203124217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166638-C-T

203124355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166502-C-T

203124595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165865-G-T

203124942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165558-A-G

203124956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165545-G-A

203124982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165518-T-C

203124998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165501-G-A

203126620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134164220-G-A

http://identifiers.org/hco/1/GRCh38#203126979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134163903-C-A

http://identifiers.org/hco/1/GRCh38#203127042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134163862-C-A

203127042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163862-C-T

203127066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163838-A-T

203127086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163819-A-G

203127101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163802-G-T

203127362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134163531-G-A

203127362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134163531-G-C

203127362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134163531-G-T

203127387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134163501-G-A

203127387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134163501-G-T

203127490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 134163435-C-T

203127504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163421-G-A

203127504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163421-G-T

203127567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163337-G-A

203127643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163262-G-T

http://identifiers.org/hco/1/GRCh38#203127692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134163213-C-A

203127692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163213-C-T

http://identifiers.org/hco/1/GRCh38#203127696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134163209-C-A

203127714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134163179-A-G

203127746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134163147-G-T

203127905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134162989-C-G

203127905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134162989-C-T

203127989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134162913-A-G

http://identifiers.org/hco/1/GRCh38#203128058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134162843-C-A

203128141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162759-G-A

203128141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162759-G-T

http://identifiers.org/hco/1/GRCh38#203128328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#134162567-C-A

203128328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134162567-C-T

203128413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 134162486-G-A

http://identifiers.org/hco/1/GRCh38#203128478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134162420-A-C

203128478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134162420-A-G

203128478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134162420-A-T

203129190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 134161743-C-G

203129190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 134161743-C-T

203129285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161647-G-A

203129293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161639-T-C

http://identifiers.org/hco/1/GRCh38#203129336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134161588-C-A

203129336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161588-C-T

http://identifiers.org/hco/1/GRCh38#203129395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134161530-C-A

203129395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161530-C-G

203129395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161530-C-T

203129484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161429-T-C

203129542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161371-G-A

203129542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161371-G-C

203129542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161371-G-T

http://identifiers.org/hco/1/GRCh38#203129543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134161370-C-A

203129543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161370-C-T

203129545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: 134161368-A-G

http://identifiers.org/hco/1/GRCh38#203129605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134161320-A-C

http://identifiers.org/hco/1/GRCh38#203129665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134161258-C-A

203129665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134161258-C-G

203129665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134161258-C-T

203129692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134161231-T-C

203129692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134161231-T-G

203129717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161206-G-A

203129717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161206-G-T

http://identifiers.org/hco/1/GRCh38#203129771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134161153-C-A

203129771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161153-C-G

203130512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160416-G-A

203130688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160248-A-T

203131103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159851-T-G

203131215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159743-C-T

203131411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159578-T-C

203131603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159408-C-T

203131616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159395-C-T

203131648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159377-T-G

203131717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159321-A-T

203131718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159320-T-C

203131894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159163-A-G

203131930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159127-G-A

203132180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134158902-C-T

203133564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134158239-A-G

203133802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134158024-G-A

http://identifiers.org/hco/1/GRCh38#203133890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134157945-C-A

203134460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157494-G-A

203134860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157117-A-G

203134998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156979-T-C

203135157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156820-G-C

203135242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156724-A-G

203135765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156265-A-G

203135923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156117-C-T

203135948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156093-C-T

203136002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156005-G-A

203136224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155794-G-A

203136304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155715-G-A

203136418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155636-A-G

203137549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154460-G-A

203137735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154293-A-G

203139261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134153071-G-A

203139312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134153025-G-A

http://identifiers.org/hco/1/GRCh38#203139444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134152942-C-A

203139444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152942-C-T

203139445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152941-G-A

203139507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152876-G-A

203139655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152732-G-A

203140339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152532-T-G

203140545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152413-C-T

203140746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152260-G-T

203140941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152084-T-C

203140973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152066-G-A

http://identifiers.org/hco/1/GRCh38#203141096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134151962-A-C

203141181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151896-G-A

203141442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151684-T-C

203141618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151547-T-G

203141948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151344-C-T

203142133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151200-G-A

203142390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150926-A-G

203142598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150753-G-A

203142696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150674-G-A

http://identifiers.org/hco/1/GRCh38#203142899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134150489-C-A

203142899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150489-C-T

203142922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150468-C-T

http://identifiers.org/hco/1/GRCh38#203144571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134147832-C-A

203144712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134147707-G-T

203144768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134147667-A-G

203145321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146972-C-T

203145389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146908-G-A

203145817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146687-T-G

203145832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146672-C-T

203146033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146494-C-G

203146132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146379-G-C

http://identifiers.org/hco/1/GRCh38#203146133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134146378-C-A

http://identifiers.org/hco/1/GRCh38#203146218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134146336-C-A

203146218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146336-C-T

203146649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146101-G-A

203146740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146004-C-T

203147458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145022-A-G

203147499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134144982-G-T

203147538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134144943-T-A

203147685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134144799-A-G

203147696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134144788-A-G

203147725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134144760-A-G

203149175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143887-G-A

203149175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143887-G-C

203149229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143832-G-A

203149270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143791-C-G

203149401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143661-C-T

203149674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143417-G-C

203149711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143378-G-A

http://identifiers.org/hco/1/GRCh38#203149854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134143232-A-C

203149912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142553-A-G

203149956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142496-G-T

203149966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 134142486-T-C

203150008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134142446-A-G

203150135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142359-G-T

http://identifiers.org/hco/1/GRCh38#203150153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134142343-C-A

203150171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142326-G-T

http://identifiers.org/hco/1/GRCh38#203150491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134142134-A-C

203150491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142134-A-G

203150514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142109-G-T

203150535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142088-T-C

203150590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142033-G-A

203150590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142033-G-T

203150607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142016-G-A

203150664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134141972-G-T

203150715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134141931-G-A

203150715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134141931-G-T

203150716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134141930-C-T

http://identifiers.org/hco/1/GRCh38#203150833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134141843-C-A

203150849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141827-G-A

203150849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141827-G-T

203150856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141820-T-A

203150856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141820-T-C

203150857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141819-G-A

http://identifiers.org/hco/1/GRCh38#203150858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134141818-C-A

203150858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141818-C-T

203150917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141786-G-A

203150917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141786-G-T

203150936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141764-C-T

203150963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141728-A-G

203150968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141723-A-G

203151559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141216-G-A

203152041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140959-A-G

203152267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140743-G-A

203152274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140724-A-G

http://identifiers.org/hco/1/GRCh38#203152408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134140614-C-A

203152414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140608-A-G

203152424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140598-G-T

203152441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134140581-T-A

203152443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134140579-A-G

203152464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140553-G-A

203152464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140553-G-T

http://identifiers.org/hco/1/GRCh38#203152477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134140540-C-A

203152494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140507-T-A

203152506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140497-C-T

203152539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140461-C-T

http://identifiers.org/hco/1/GRCh38#203152670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134140349-C-A

203152710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 134140310-G-A

203152860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134140184-G-T

http://identifiers.org/hco/1/GRCh38#203152862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#134140182-C-A

http://identifiers.org/hco/1/GRCh38#203152888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134140158-C-A

203152888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140158-C-T

203152898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140148-G-T

http://identifiers.org/hco/1/GRCh38#203152962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134140077-A-C

203153061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139978-C-T

203153210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139844-C-T

203153548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139518-C-T

203153550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139516-C-T

203153568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139495-G-A

203153787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139280-T-C

203153920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139146-G-A

203153947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139119-A-G

203154085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138975-T-G

203154144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138918-T-A

203154165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138897-C-T

203154173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138889-C-T

203154373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138815-A-G

203154529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138665-G-A

203154675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138550-C-T

http://identifiers.org/hco/1/GRCh38#203154793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134138452-C-A

203155208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138178-G-A

203156117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137366-A-G

203156306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137225-G-C

203156346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137170-T-C

203156659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136929-G-A

http://identifiers.org/hco/1/GRCh38#203161322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134135440-C-A

203161322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135440-C-G

203161871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135042-G-A

203162232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134796-C-T

203162287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134742-C-T

203162303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134726-G-A

203162894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134189-C-T

http://identifiers.org/hco/1/GRCh38#203163095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134133997-A-C

203163100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133992-G-A

203163106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133986-A-G

203163218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133879-G-A

203163283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133808-A-T

203163315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133784-G-A

203163422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133673-G-A

203163424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133671-A-G

203163541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133586-T-C

203163543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133580-T-C

203163554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133569-T-C

203163577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133546-G-A

http://identifiers.org/hco/1/GRCh38#203164324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134132301-A-C

203164524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132119-G-T

203164634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132028-G-A

203164953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131784-G-T

203165105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134131464-C-G

203165151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134131428-G-A

http://identifiers.org/hco/1/GRCh38#203165179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134131409-C-A

203165179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134131409-C-G

203165179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134131409-C-T

203165213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 134131382-G-A

203165213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 134131382-G-C

203165251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134131336-T-C

203165295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134131292-G-A

203165295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134131292-G-T

203165499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134131088-C-T

203165613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134130974-A-G

203166070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134130511-T-A

203166070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134130511-T-C

http://identifiers.org/hco/1/GRCh38#203166082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134130499-A-C

203166109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134130469-A-G

203166111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134130467-G-A

203166138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134130442-G-A

203166138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134130442-G-T

http://identifiers.org/hco/1/GRCh38#203166331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134130305-C-A

203166434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134130201-A-G

203166491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134130149-A-G

203166491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134130149-A-T

203166605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134130030-C-T

http://identifiers.org/hco/1/GRCh38#203166701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#134129937-C-A

203166701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134129937-C-G

203166701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134129937-C-T

203166716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134129927-G-T

http://identifiers.org/hco/1/GRCh38#203166792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#134129856-C-A

203166792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134129856-C-T

203166840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134129811-G-A

203166840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134129811-G-C

203166840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134129811-G-T

http://identifiers.org/hco/1/GRCh38#203166864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134129785-C-A

203166864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129785-C-T

203166867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129782-G-C

203166867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129782-G-T

203166879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129771-G-A

203166879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129771-G-T

203166887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129763-A-G

203166888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129762-G-A

203166927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129724-G-T

http://identifiers.org/hco/1/GRCh38#203167000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#134129623-C-A

203167274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129471-C-T

203167371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129372-A-G

203167371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129372-A-T

203167377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 262
most severe consequence: 3 prime UTR variant
orthologous variants: 134129367-A-G