173168689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184225-C-G

173169181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185665-A-G

http://identifiers.org/hco/2/GRCh38#173169956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72186052-C-A

173170382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186467-C-T

173170792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186896-C-T

http://identifiers.org/hco/2/GRCh38#173170883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72186986-A-C

173170901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187004-G-C

173171181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187262-C-T

173171226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187307-C-T

173171644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188101-G-A

173172183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188528-A-G

173172462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188750-T-A

173172591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188813-A-G

173172654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188860-G-A

173172820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189026-G-A

173172820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189026-G-T

173173259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189252-C-T

173173290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189283-C-T

173173375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189366-T-C

173173680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189664-C-T

173173710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189691-C-T

173174137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191147-A-G

173182813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194941-T-A

173182980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195098-T-C

173183009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195124-T-C

http://identifiers.org/hco/2/GRCh38#173183070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72195185-C-A

173183305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195435-T-C

173183365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195484-C-G

173183365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195484-C-T

173183546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195644-C-T

173183619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195703-A-T

173183625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195709-C-T

173183627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195711-T-C

173183692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195775-C-T

173183991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196028-C-T

173184222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196299-T-C

173184249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196326-T-C

173184333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196387-A-G

173184539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72196568-T-C

173184565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72196585-A-G

173185570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196950-C-T

173185586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196966-A-G

173185628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72197008-G-A

http://identifiers.org/hco/2/GRCh38#173185707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72197083-C-A

173185707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72197083-C-G

173186107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72197430-T-C

173186833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198156-A-G

173186874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198197-G-A

173187086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198394-C-G

173187178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198438-C-T

173187529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198722-T-C

173187666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198853-T-C

173187670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198857-T-C

http://identifiers.org/hco/2/GRCh38#173187699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72198885-C-A

173187724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198909-T-A

http://identifiers.org/hco/2/GRCh38#173187738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72198921-C-A

173187738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198921-C-T

173188068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199251-A-G

173188229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199413-C-T

173188247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199431-A-G

173188329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199485-G-A

173188502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199673-C-T

173188999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200074-A-G

173189861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200960-G-A

173189968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201071-A-G

173190469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201534-C-T

173190841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202022-A-G

173190860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202038-T-A

173190879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202057-T-C

173190911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72202087-T-C

173191032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72202207-T-G

173191239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202414-A-G

http://identifiers.org/hco/2/GRCh38#173191299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72202463-C-A

173191299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202463-C-T

173191362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202530-G-A

173191362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202530-G-T

173191437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202603-G-A

173191457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202614-T-C

http://identifiers.org/hco/2/GRCh38#173191461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72202618-A-C

173191490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202647-T-C

173191596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202750-G-A

173191743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202845-G-A

173191743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202845-G-T

173191765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202870-G-C

173191795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202894-C-G

http://identifiers.org/hco/2/GRCh38#173192617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72203539-A-C

173192630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203552-A-T

http://identifiers.org/hco/2/GRCh38#173192668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72203582-C-A

173192803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203669-C-T

http://identifiers.org/hco/2/GRCh38#173193016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72203872-C-A

173193047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72203916-G-A

173193057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 72203926-C-G

173193101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203955-C-T

173193131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203970-G-T

173193154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203993-T-C

173193180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204018-A-G

173193320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204101-C-T

173193455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204238-T-C

173193637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204393-T-C

173193806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204554-T-C

173193932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204787-C-G

173193932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204787-C-T

173194375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205526-A-G

173194400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205551-A-T

173194545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205691-T-A

173194649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205752-T-C

http://identifiers.org/hco/2/GRCh38#173194710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72205797-A-C

http://identifiers.org/hco/2/GRCh38#173194796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72205862-C-A

173194995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205970-T-C

173195004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205978-T-C

173195794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72206715-A-T

173196316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207177-T-G

173196354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207216-T-C

http://identifiers.org/hco/2/GRCh38#173196549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72207455-C-A

173196612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207518-C-T

173196767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207671-T-A

173196768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207672-C-G

173196768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207672-C-T

173196951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207858-G-A

173196994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207898-T-C

173197112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208010-T-C

173197240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208252-G-T

http://identifiers.org/hco/2/GRCh38#173197339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72208346-A-C

173197548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208517-G-A

173197556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208525-G-A

173198409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72209361-T-C

173199436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210381-G-A

173199589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210532-A-G

http://identifiers.org/hco/2/GRCh38#173200049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72210872-C-A

173201476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211919-C-G

173201853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212489-C-T

173202011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212623-T-G

173202058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212671-T-A

173202141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212752-C-T

173202248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212854-T-G

http://identifiers.org/hco/2/GRCh38#173202707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72213398-A-C

http://identifiers.org/hco/2/GRCh38#173202844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72213552-A-C

173202898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213596-G-A

173202898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213596-G-C

173203009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213703-G-A

http://identifiers.org/hco/2/GRCh38#173203173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72213873-C-A

173203758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214438-C-G

173203810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72214489-A-G

173203840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72214519-G-A

173203906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214575-T-C

173204013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214605-G-A

173204013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214605-G-C

173204013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214605-G-T

http://identifiers.org/hco/2/GRCh38#173204018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72214610-C-A

173204077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214629-C-G

173204531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215080-G-A

http://identifiers.org/hco/2/GRCh38#173205102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72215572-C-A

173205102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215572-C-G

173205102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215572-C-T

173205270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215652-G-C

173205472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215836-C-T

173205815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216118-T-C

173205836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216138-G-T

173206193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216468-T-C

173206454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216718-G-A

http://identifiers.org/hco/2/GRCh38#173206542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72216792-A-C

173206543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216793-A-G

173206695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216915-T-C

173206714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216934-A-G

173206757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216980-A-G

173206815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216998-C-G

173207068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217146-T-C

173207111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217189-G-C

173207206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217257-A-T

173207612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72217524-G-A

173207612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72217524-G-T

http://identifiers.org/hco/2/GRCh38#173207703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72217613-C-A

173207703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217613-C-T

173207725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217801-T-G

http://identifiers.org/hco/2/GRCh38#173207771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72217847-C-A

173207771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217847-C-T

173207792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217867-T-A

173207914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217970-A-G

http://identifiers.org/hco/2/GRCh38#173208175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72218255-A-C

173208926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219228-T-A

173208927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219229-A-G

http://identifiers.org/hco/2/GRCh38#173209684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72219773-C-A

173209684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72219773-C-T

http://identifiers.org/hco/2/GRCh38#173209695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72219784-C-A

http://identifiers.org/hco/2/GRCh38#173209700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72219789-C-A

173209700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72219789-C-G

173209700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72219789-C-T

173209999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220049-G-A

173209999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220049-G-C

173209999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220049-G-T

173210027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220070-T-C

http://identifiers.org/hco/2/GRCh38#173210033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72220076-C-A

http://identifiers.org/hco/2/GRCh38#173210041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72220084-C-A

173210041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220084-C-T

173210078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220095-G-A

173210078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220095-G-C

173210078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220095-G-T

173210114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220110-G-A

173210386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220204-A-G

173210470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220231-G-A

173210470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220231-G-C

http://identifiers.org/hco/2/GRCh38#173210748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72220487-C-A

173210748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72220487-C-T

173210756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72220495-G-A

173210756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72220495-G-C

http://identifiers.org/hco/2/GRCh38#173210761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72220499-C-A

173210761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72220499-C-T

173210772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72220510-C-T

173210839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72220564-T-C

173210839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72220564-T-G

173210934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220667-G-T

173211047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72220781-T-C

173213124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224694-G-C

173213148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224712-G-T

173213431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225075-G-C

173213463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225111-A-G

173213511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225154-G-A

173213526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225169-C-G

173213611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225264-T-C

173214264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225780-C-T

173214299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72225799-C-T

173214356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72225866-T-C

http://identifiers.org/hco/2/GRCh38#173214376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72225890-A-C

173214514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226025-C-G

173214586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226095-T-C

173214869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226341-G-T

173214945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226393-G-A

173214950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226398-G-A

173215033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226481-C-T

173215062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226511-G-A

173215062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226511-G-C

173215070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226519-C-G

173215184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226632-T-G

173215218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226666-C-T

173215241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226687-C-T

173215571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227015-C-G

173215737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72227135-G-A

173215935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227299-T-C

173216003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227360-A-G

173216189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227566-A-G

173216189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227566-A-T

173216259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227634-A-G

173216684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228315-A-T

173216894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228414-C-G

173217017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228538-G-T

http://identifiers.org/hco/2/GRCh38#173217041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72228561-C-A

173217065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228585-T-C

173217238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72228757-G-A

173217238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72228757-G-T

173217313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228819-G-A

173217313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228819-G-T

173217321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228827-G-A

173217321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228827-G-T

http://identifiers.org/hco/2/GRCh38#173217388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72228896-C-A

173217388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228896-C-G

173217388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228896-C-T

http://identifiers.org/hco/2/GRCh38#173217606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72229137-C-A

173218273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229720-T-C

173218285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229735-G-A

173218302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229752-T-C

173218841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230262-G-A

173218845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230266-T-C

173218884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230292-G-A

173218884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230292-G-T

173218941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230348-T-C

173219173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230576-G-C

173219204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230602-A-G

173219286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230677-G-A

173219364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230751-A-G

173219735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231086-G-A

173219787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231109-G-T

173219865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231209-A-G

173219865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231209-A-T

173219885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231229-A-G

173220448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231645-T-G

173220472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231664-T-C

173220775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231990-T-A

173220907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72232124-T-G

173221359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72232542-G-A

173221601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72232811-T-G

173221606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72232818-A-G

173221967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233206-T-C

173222183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233259-G-A

173222183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233259-G-T

173222547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233592-A-G

173222576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233617-G-A

173222743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233772-A-G

173222905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233943-G-C

http://identifiers.org/hco/2/GRCh38#173222918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72233954-A-C

173223025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234186-G-T

173223038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234198-A-G

173223071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234229-T-A

173223163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234322-G-A

173223163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234322-G-T

http://identifiers.org/hco/2/GRCh38#173223276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72234359-C-A

173223276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234359-C-G

173223299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234383-T-C

173223333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234415-G-A

173223438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234496-A-G

http://identifiers.org/hco/2/GRCh38#173223643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72234711-C-A

173223643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234711-C-T

173223662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234729-G-A

173223685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234749-A-G

173223710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234764-A-G

http://identifiers.org/hco/2/GRCh38#173223722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72234778-C-A

173223722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234778-C-T

173224047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235053-G-T

173224066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235072-G-A

173224066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235072-G-T

173224067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235073-C-T

173224102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235080-G-T

173224125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235106-A-G

http://identifiers.org/hco/2/GRCh38#173224133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72235114-C-A

173224171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235151-G-A

173224485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235417-T-G

173224563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235494-A-G

173224656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235584-T-A

173224656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235584-T-C

173224724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235640-T-G

http://identifiers.org/hco/2/GRCh38#173224945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72235858-C-A

173224945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235858-C-T

173225047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235959-T-A

173225054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235964-A-G

173225058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235968-A-G

173225097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235993-A-T

http://identifiers.org/hco/2/GRCh38#173225132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72236025-C-A

173225132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236025-C-T

http://identifiers.org/hco/2/GRCh38#173225166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72236058-C-A

173225531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236160-T-C

http://identifiers.org/hco/2/GRCh38#173225774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72236304-A-C

173225774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236304-A-G

173225789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236327-T-A

173225818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236354-T-C

173225900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236416-T-A

173225900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236416-T-C

173225900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236416-T-G

173225971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236471-T-C

173225971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236471-T-G

173226202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236719-G-C

173226202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72236719-G-T

173226269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237006-A-G

http://identifiers.org/hco/2/GRCh38#173226379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72237120-C-A

173226412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237154-A-G

http://identifiers.org/hco/2/GRCh38#173226514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72237248-C-A

173226514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237248-C-G

173226514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237248-C-T

173226525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237259-T-C

173226531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237265-G-A

http://identifiers.org/hco/2/GRCh38#173226631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72237363-C-A

173226668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237402-T-C

http://identifiers.org/hco/2/GRCh38#173227036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72237736-C-A

http://identifiers.org/hco/2/GRCh38#173227205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72237905-C-A

173227683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238379-A-G

173227863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238564-T-C

173228367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239071-G-A

173228408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239112-C-T

173228935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239835-G-C

173228961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239856-T-C

173229650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240453-T-A

173229650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240453-T-C

173229650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240453-T-G

http://identifiers.org/hco/2/GRCh38#173229741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72240544-C-A

173229741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72240544-C-G

173229852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240651-T-C

173230185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240709-G-C

173230521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241013-T-C

http://identifiers.org/hco/2/GRCh38#173230607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72241066-A-C

173230678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241136-A-G

173230703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241161-T-A

173231097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241286-A-T

173231216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241413-G-T

173231347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241521-A-G

173231536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241666-T-G

173231615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241743-G-A

173231761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241884-G-A

173231764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241887-G-A

173231809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241933-T-C

http://identifiers.org/hco/2/GRCh38#173231887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72242001-C-A

173232094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242182-A-G

173232094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242182-A-T

173232194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 72242276-T-C

http://identifiers.org/hco/2/GRCh38#173232244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72242326-C-A

173232270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242368-T-G

173232430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242525-G-T

173232468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242563-G-C

173233000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242762-C-T

173234294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72243791-T-G

173234531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244020-G-A

173234752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244198-T-C

173234847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244287-G-A

173234870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244300-A-G

173237830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72246052-G-A

173238317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72246826-T-C

173238317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72246826-T-G

173238426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72246938-A-G

http://identifiers.org/hco/2/GRCh38#173238550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72247057-C-A

173238550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247057-C-T

173238585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247091-G-T

173238602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247108-C-G

173238787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247295-C-T

173238904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247691-G-A

http://identifiers.org/hco/2/GRCh38#173239089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72247848-A-C

173239175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247927-G-C

173239196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247947-G-C

173239274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248024-A-T

173239341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248231-T-A

173239341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248231-T-C

173239346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248236-T-A

173239346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248236-T-C

http://identifiers.org/hco/2/GRCh38#173239368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72248264-C-A

173239368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248264-C-T

173239888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248724-C-T

173239921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248757-C-T

173239922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248758-A-G

http://identifiers.org/hco/2/GRCh38#173239931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72248767-A-C

173239936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248772-T-A

173240003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248834-G-C

173242010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250151-G-T

http://identifiers.org/hco/2/GRCh38#173242165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72250359-C-A

http://identifiers.org/hco/2/GRCh38#173242172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72250363-A-C

173242178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250369-T-A

173242502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250433-A-T

173242675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250591-G-A

173243150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250728-T-C

173243367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250929-G-A

173243499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251036-G-A

173243557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251076-A-G

173243558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251077-T-C

173243967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251163-G-A

173244170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251345-G-C

http://identifiers.org/hco/2/GRCh38#173244184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72251358-A-C

173244460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251606-G-A

173244503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251649-A-G

173245045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252148-G-A

173245242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252738-C-T

173245332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252822-G-A

173245372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252862-T-C

173245637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253135-T-C

173246022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253317-G-C

173246268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253553-T-C

173246355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253637-A-G

173246438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253718-G-A

173246662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253937-A-G

173247015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254195-T-C

173247075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254256-C-G

173247146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254320-A-G

173247291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254433-G-T

173247346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254485-T-C

173248588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255185-G-A

173248588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255185-G-C

173248733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255319-T-C

173248734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255320-C-G

173248739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255325-T-G

http://identifiers.org/hco/2/GRCh38#173248886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72255840-A-C

173249017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255950-T-C

173249818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256661-T-C

173249884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256725-A-G

173249897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256738-C-G

173250757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72257592-G-A

http://identifiers.org/hco/2/GRCh38#173251363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72258166-C-A

173251363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72258166-C-T

173251731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72258493-T-C

173252574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259289-G-C

173252597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259312-G-A

http://identifiers.org/hco/2/GRCh38#173252599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72259314-A-C

173252599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259314-A-G

173252628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259343-C-T

173252634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259349-C-T

173257240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72262448-G-A

173257368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72262572-A-G

173257403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72262597-A-G

173257967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263081-G-A

173257967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263081-G-T

173258251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263373-G-A

173258341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263472-A-G

173258341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263472-A-T

173258352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263483-G-A

173258362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263497-T-C

173258564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263581-T-G

173258657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263671-G-A

173258657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263671-G-T

173258778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72263791-C-T

173258779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72263792-T-G

173258975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263989-T-A

173259172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264187-T-G

173259187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264201-T-G

173259206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264256-T-A

173259782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264862-C-G

173259837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264915-G-A

173260814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265202-C-T

173260828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265294-G-C

173260942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265454-G-C

173260942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265454-G-T

http://identifiers.org/hco/2/GRCh38#173260961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72265473-C-A

http://identifiers.org/hco/2/GRCh38#173261006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72265518-A-C

173261006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265518-A-G

173261042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265554-A-T

173261100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72265612-C-G

http://identifiers.org/hco/2/GRCh38#173261206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72265718-C-A

173261527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266780-G-C

173262090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266993-T-C

173262103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267016-T-C

http://identifiers.org/hco/2/GRCh38#173262142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72267053-A-C

173262142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267053-A-G

173262237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267154-G-C

173263180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267881-G-A

173263180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267881-G-T

173263241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267939-G-A

173263241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267939-G-T

173263302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268004-G-T

173263399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268079-G-C

173263924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268726-T-C

173266102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72271628-C-T

http://identifiers.org/hco/2/GRCh38#173266405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72271931-A-C

173266567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272099-C-T

173266616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272148-A-G

http://identifiers.org/hco/2/GRCh38#173266744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72272276-C-A

173266744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272276-C-T

http://identifiers.org/hco/2/GRCh38#173266778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72272311-C-A

173266778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272311-C-G

173266778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272311-C-T

http://identifiers.org/hco/2/GRCh38#173266779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72272312-A-C

173266779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272312-A-G

173266779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272312-A-T

173266878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272398-G-T

173267001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272525-T-C

173267218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72272721-A-G

http://identifiers.org/hco/2/GRCh38#173267481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72272912-C-A

http://identifiers.org/hco/2/GRCh38#173267681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72273107-C-A

http://identifiers.org/hco/2/GRCh38#173267682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72273108-C-A

http://identifiers.org/hco/2/GRCh38#173267767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72273184-C-A

173267791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72273206-T-A

173267835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72273242-A-G

173267846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72273250-G-T

173267893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72273279-C-T

http://identifiers.org/hco/2/GRCh38#173267896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#72273282-C-A

173267911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72273299-G-T

173268026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72273435-A-G

173268027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72273436-G-A

173268027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72273436-G-T

173268745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72273680-A-T

173268774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72273698-A-G

173269142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72274057-G-T

173270479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72276213-T-C

173270981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72276687-C-T

173271118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72276752-C-T

173271216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72276806-T-C

173271662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277007-G-A

173271679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277024-G-A

173271679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277024-G-T

173271682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277027-G-C

http://identifiers.org/hco/2/GRCh38#173271700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72277045-C-A

173271759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277090-T-A

173272051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277323-G-A

173272127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277388-A-G

173272129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277390-G-C

173272241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277534-A-G

173272298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277630-C-T

173273135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278135-C-T

173273136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278136-G-A

173273178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278164-T-G

173273220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278206-T-C

173273380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278363-T-C

173273485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278467-G-C

173273626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278624-A-T

173273644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278652-C-T

173273647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278655-G-A

http://identifiers.org/hco/2/GRCh38#173273923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72278783-A-C

http://identifiers.org/hco/2/GRCh38#173274233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72279189-A-C

173274334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72279289-C-T

173279295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72282352-C-T

173279403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72282623-A-T

173279630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72282732-C-G

173279730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72282808-G-C

173279861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72282936-A-G

173280049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283102-C-T

173280223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283269-C-T

173280257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283302-T-C

173280258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283303-A-T

173280294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283339-T-C

173280387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283431-A-G

173281509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284475-C-G

173281509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27935
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284475-C-T