177654874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75839978-G-A

http://identifiers.org/hco/2/GRCh38#177654880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75839984-A-C

177655170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75840228-T-C

177655338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75840397-G-T

177655962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75840815-T-C

http://identifiers.org/hco/2/GRCh38#177656018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75840874-A-C

177656018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75840874-A-G

177656655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75841178-T-C

177656753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75841275-T-C

177656871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75841400-C-T

177657016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75841552-T-C

http://identifiers.org/hco/2/GRCh38#177657086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75841707-C-A

177657103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75841724-G-A

177657257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75841872-T-C

http://identifiers.org/hco/2/GRCh38#177657262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75841877-C-A

177657711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842194-T-G

177657853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842342-G-A

177657890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842368-T-C

177657905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842373-G-A

177658068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842500-C-G

177658597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842531-A-G

177658703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842661-C-T

177658716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842674-T-A

177658791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75842822-C-T

177659892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844267-T-A

177659892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844267-T-C

177659963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844337-T-C

177660097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844413-T-C

177660104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844420-T-C

177660307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844543-G-T

177660376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844603-T-C

177660452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844669-A-G

177660572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844836-C-T

177660661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75844925-A-G

177660866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845107-A-G

177660950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845185-T-C

177661129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845342-G-A

177661296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845520-C-T

http://identifiers.org/hco/2/GRCh38#177661303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75845527-C-A

177661430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845672-C-T

177661442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845684-G-A

177661570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845811-C-T

177661714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75845954-G-C

177661768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75846010-T-C

177661816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75846261-C-T

http://identifiers.org/hco/2/GRCh38#177662114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75846545-C-A

http://identifiers.org/hco/2/GRCh38#177662157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75846588-A-C

http://identifiers.org/hco/2/GRCh38#177662508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75846827-A-C

177662908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75847200-T-C

http://identifiers.org/hco/2/GRCh38#177663087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75847370-C-A

177663779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848092-G-A

177663779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848092-G-T

177663814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848120-T-A

177663814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848120-T-C

177663814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848120-T-G

177663966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848278-G-A

177663966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848278-G-T

177663987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848299-C-G

177663987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848299-C-T

http://identifiers.org/hco/2/GRCh38#177664050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75848349-C-A

177664050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848349-C-T

177664072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848367-T-C

http://identifiers.org/hco/2/GRCh38#177664083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75848378-A-C

177664083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848378-A-G

177664401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848715-T-C

177664521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75848828-T-C

http://identifiers.org/hco/2/GRCh38#177664600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75848905-A-C

http://identifiers.org/hco/2/GRCh38#177664760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75849054-C-A

177664950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75849216-G-T

177664963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75849229-T-A

177665035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75849305-C-G

177665140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75849384-G-C

177665180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75849425-G-A

177667684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75851171-G-A

177667694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75851181-C-T

177668194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75851601-A-G

177668220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75851626-G-A

http://identifiers.org/hco/2/GRCh38#177668595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75851991-C-A

177668777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75852174-A-T

http://identifiers.org/hco/2/GRCh38#177668987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75852384-A-C

177668987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75852384-A-G

http://identifiers.org/hco/2/GRCh38#177669021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75852418-C-A

177669134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75852535-C-T

177669169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75852568-C-T

http://identifiers.org/hco/2/GRCh38#177669416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75852977-C-A

177669416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75852977-C-T

177669446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853006-A-G

177669473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853035-T-C

177669590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853152-T-A

177669595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853157-G-A

177669595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853157-G-T

177669635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853196-T-G

177669649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853210-G-A

177669649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853210-G-T

177670476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853399-G-A

177670476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853399-G-T

177670555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853480-C-T

177670578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853502-G-A

177670578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853502-G-T

177670750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853874-A-G

177670756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853880-T-A

177670860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75853995-T-G

177670924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854055-C-T

177670984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854109-C-T

http://identifiers.org/hco/2/GRCh38#177671131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75854243-A-C

177671168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854271-G-A

177671174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854277-G-A

http://identifiers.org/hco/2/GRCh38#177671210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75854305-A-C

177671259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854332-C-G

177671259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854332-C-T

177671401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854502-A-G

177671417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75854518-T-G

177672142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75855485-C-T

177672146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75855489-A-G

177672146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75855489-A-T

177672402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75855684-G-C

177672565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75855913-T-C

177672662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75856011-C-T

177672749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75856096-G-A

177672926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75856279-T-C

http://identifiers.org/hco/2/GRCh38#177673295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75856829-C-A

177673295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75856829-C-T

177673373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75856897-C-T

177673383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75856972-C-G

177673398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75856987-G-T

177673510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75857081-C-T

177673514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75857085-T-C

177673561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75857152-G-C

177673675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75857264-G-A

177673827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75857408-T-C

177673836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75857417-T-C

177674371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75858420-G-A

http://identifiers.org/hco/2/GRCh38#177674489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75858545-C-A

177674557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858610-C-T

177674617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858719-T-A

177674636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858738-G-A

http://identifiers.org/hco/2/GRCh38#177674703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75858824-A-C

177674716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858837-G-C

177674789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858898-C-T

177674845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858953-T-C

177674850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858958-C-G

177674850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75858958-C-T

177674867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75859118-C-T

http://identifiers.org/hco/2/GRCh38#177675418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75859584-C-A

177675418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75859584-C-T

http://identifiers.org/hco/2/GRCh38#177675596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75859761-A-C

177675596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75859761-A-G

177675596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75859761-A-T

177675621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75859778-G-T

177675654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75859810-C-G

177675654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75859810-C-T

177675775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75859938-G-A

177675829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75859992-T-C

177675863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860019-A-G

177675864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860020-T-C

177675917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 75860071-C-G

177675939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860086-G-A

177675939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860086-G-C

177675939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860086-G-T

http://identifiers.org/hco/2/GRCh38#177675951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75860101-A-C

177675962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860112-A-G

177675963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860113-G-A

177675976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860126-T-A

177675976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860126-T-C

http://identifiers.org/hco/2/GRCh38#177675985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75860135-A-C

177675994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860144-T-C

177676080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860226-G-A

177676080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860226-G-C

177676080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75860226-G-T

177676157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860299-G-A

177676157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860299-G-T

177676213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860354-A-T

177676392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860507-T-C

177676392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860507-T-G

177676630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860706-C-G

177676919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75860971-G-A

177676951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861003-A-G

177677039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861087-A-G

177677089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861145-A-G

177680792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861233-A-G

177680792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861233-A-T

177680798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861239-A-G

177680885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75861327-A-G

177680934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861373-A-G

177680941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861380-A-G

177681157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861592-A-G

177681306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861714-G-T

177681510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861909-G-A

177681533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75861933-A-G

177682570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75862162-A-G

177682814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75862391-G-A

177683028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75862544-G-T

177683219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75862719-G-T

177683322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75862813-T-C

177683378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75862870-T-A

177683402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75862893-T-C

177683405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75862896-T-C

177683407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75862898-C-G

177683853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75862988-G-T

177683871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75863004-G-A

177684496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75863935-C-T

177684594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864025-C-T

177684599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864030-A-G

177684605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864036-G-T

177684621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864053-C-T

177684751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864171-T-G

177684789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864212-A-G

177685003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864404-T-C

http://identifiers.org/hco/2/GRCh38#177685081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75864483-C-A

177685327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75864711-C-G

177685476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75865070-A-G

177685495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75865089-G-A

177685935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75865490-C-T

177687348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866011-A-G

177687351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866014-C-G

177687385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866047-T-C

177687467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866117-G-T

177687708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866335-A-G

177687721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866348-G-A

177687744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866512-T-C

http://identifiers.org/hco/2/GRCh38#177687772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75866540-A-C

http://identifiers.org/hco/2/GRCh38#177687818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75866588-C-A

177687836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866606-G-A

177687857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866627-G-T

177688015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866673-G-T

http://identifiers.org/hco/2/GRCh38#177688040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75866697-C-A

177688040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866697-C-T

177688054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866711-G-T

177688103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866761-C-T

177688177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866836-A-G

177688236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75866887-G-T

http://identifiers.org/hco/2/GRCh38#177688246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75866897-C-A

177688552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75867199-G-C

177688573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75867220-T-G

177688953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75867607-A-T

177689067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75867723-C-T

http://identifiers.org/hco/2/GRCh38#177689527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75868101-C-A

177689527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75868101-C-T

177689862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75868528-A-G

177689936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75868589-C-T

177689938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75868591-C-G

177689938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75868591-C-T

177690107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75868752-T-C

177690207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75868851-T-C

177690715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75869341-G-A

177690715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75869341-G-C

177691299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75869928-G-A

177691386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75870043-G-C

177692233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75870680-G-A

177692320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75870768-T-A

177692359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75870840-T-C

177692547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75871077-G-A

177692584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75871127-T-G

177692763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75871296-T-C

http://identifiers.org/hco/2/GRCh38#177692907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75871421-C-A

177693298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75871931-C-T

177693407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75872039-C-T

177693548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75872173-C-T

177694386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75873014-G-A

177694392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75873020-G-C

177694395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75873023-T-A

177694482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75873109-T-A

177694582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75873215-G-C

177694640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75873276-A-T

177696441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75876630-A-T

177696912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75876753-T-C

http://identifiers.org/hco/2/GRCh38#177697161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75876979-A-C

177697180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75876998-T-C

http://identifiers.org/hco/2/GRCh38#177697227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75877013-C-A

177697227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877013-C-T

http://identifiers.org/hco/2/GRCh38#177697228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75877014-A-C

177697228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877014-A-G

177697228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877014-A-T

177697230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877016-T-A

177697230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877016-T-G

177697266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877052-T-C

http://identifiers.org/hco/2/GRCh38#177697315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75877106-C-A

177697315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877106-C-T

http://identifiers.org/hco/2/GRCh38#177697523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75877324-C-A

177697547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877575-A-T

177697751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877739-T-A

177697753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75877741-C-T

177698147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75878104-G-A

177698203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75878159-G-T

177698849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75878795-T-C

177698855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75878801-A-G

177699774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879298-G-T

177699907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879418-C-T

177700228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879701-C-G

177700244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879717-G-A

177700280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879764-C-T

177700333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879817-A-T

177700347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879853-T-C

177700347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879853-T-G

http://identifiers.org/hco/2/GRCh38#177700373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75879879-A-C

http://identifiers.org/hco/2/GRCh38#177700381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75879887-C-A

177700693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880184-A-G

177700867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880260-T-A

177700867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880260-T-C

http://identifiers.org/hco/2/GRCh38#177700948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75880329-C-A

177700974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880352-A-G

177700984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880361-A-G

177701013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880388-T-G

177701025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880399-T-C

177701037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880411-G-T

177701072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880439-A-T

177701103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75880470-A-G

177701103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75880470-A-T

177701142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75880505-G-A

177701142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75880505-G-T

177701233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880597-G-A

177701233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880597-G-T

177701242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880606-G-A

177701242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880606-G-T

177701275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880642-G-T

177701448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880769-T-A

177701464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880785-C-T

177701756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881217-T-C

177701779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881239-A-G

177701797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881256-C-T

http://identifiers.org/hco/2/GRCh38#177701844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75881295-C-A

177701844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881295-C-T

177701900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881346-C-T

177701907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881353-C-T

177701910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881356-T-C

177702115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881565-C-T

177702123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881573-G-A

177702181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881629-G-A

177702181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881629-G-C

177702342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881666-T-A

177702342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881666-T-C

http://identifiers.org/hco/2/GRCh38#177702354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75881678-C-A

http://identifiers.org/hco/2/GRCh38#177702370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75881694-A-C

177702370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881694-A-G

177702370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881694-A-T

177702377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881701-G-A

177702407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881717-A-G

177702424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881725-G-A

177702424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881725-G-T

177702455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881755-C-G

http://identifiers.org/hco/2/GRCh38#177702606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75881905-C-A

177702606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75881905-C-T

http://identifiers.org/hco/2/GRCh38#177702655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75881939-C-A

177702659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75881943-G-A

177702895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75882124-G-A

http://identifiers.org/hco/2/GRCh38#177702961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75882189-A-C

177702998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75882218-G-A

177703080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75882256-A-G

177703594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75882614-T-C

177704086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75882969-G-C

177704170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75883084-T-C

177704200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75883113-G-C

http://identifiers.org/hco/2/GRCh38#177704256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75883168-A-C

177704279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75883190-T-G

177704499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75883388-C-T

177705210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75883763-T-C

177705522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884038-G-A

177705533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884049-T-G

177705759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884274-G-A

177706074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884577-T-C

177706122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884625-G-A

177706173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884676-C-T

177706307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884823-T-G

177706423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884940-C-G

177706654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885149-A-T

177706880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885371-G-C

http://identifiers.org/hco/2/GRCh38#177706884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75885375-C-A

177707036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885513-A-T

177707428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885868-T-A

177707428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885868-T-G

177707429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885869-C-T

177707434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885874-A-G

http://identifiers.org/hco/2/GRCh38#177707437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75885875-A-C

177707652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75886075-C-G

177707652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75886075-C-T

177707751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75886157-T-C

177707783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75886188-A-G

177708093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75886501-G-A

177708674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75886591-T-C

177709212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75886977-C-T

177709558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75887284-G-A

177709752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75887448-A-T

177710057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75887747-G-A

177710115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75887806-G-A

177710135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75887827-G-A

177710356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888042-T-C

177710921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888583-C-T

177711009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888664-C-T

177711270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888909-G-C

177711440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888990-G-A

177711464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889014-A-G

177711730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889282-G-A

177711730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889282-G-C

177711747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889299-A-G

177711752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889304-C-G

177711752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889304-C-T

177712213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889720-T-C

177712346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889836-T-C

177712408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889887-A-T

177712544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75890001-G-A

177712643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75890096-A-G

177712643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75890096-A-T

177712646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75890099-A-G

177712711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75890164-G-C

177712916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75890345-G-C

177717143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75893819-C-G

177717172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75893848-G-A

http://identifiers.org/hco/2/GRCh38#177717274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75893950-A-C

http://identifiers.org/hco/2/GRCh38#177717291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75893967-C-A

177717422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75894096-C-T

177717429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75894102-A-T

177717560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75894222-C-T

177717819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75894471-G-T

177717963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75894582-T-C

177718099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75894717-G-C

177718494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895016-T-C

177718498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895020-T-C

177718502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895024-G-A

177718626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895151-C-T

177718683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895206-A-G

177718743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895254-T-G

177719745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895943-G-C

http://identifiers.org/hco/2/GRCh38#177719960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75896122-A-C

177720155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896229-G-A

177720179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896251-G-C

177720326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896401-C-T

177720548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896593-G-A

http://identifiers.org/hco/2/GRCh38#177720619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75896654-C-A

177720628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896662-C-G

http://identifiers.org/hco/2/GRCh38#177720689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75896712-C-A

177720743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896756-T-C

177721013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75897032-T-C

177721608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75897962-T-C

http://identifiers.org/hco/2/GRCh38#177721616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75897969-C-A

177721616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75897969-C-T

177721620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75897973-A-T

http://identifiers.org/hco/2/GRCh38#177722358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75898700-A-C

177722370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898712-G-A

177722370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898712-G-T

177722576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898919-G-A

177722606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898948-A-T

177722620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898962-G-A

177722620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898962-G-C

177722630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898972-T-A

177722672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899013-T-C

177722829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899178-A-G

177722854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899203-G-C

177722888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899230-A-T

177722898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899240-T-C

177722983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899309-T-C

177722983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899309-T-G

http://identifiers.org/hco/2/GRCh38#177723169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#75899487-C-A