96593516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41260905-G-T

http://identifiers.org/hco/10/GRCh38#96593648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41261003-C-A

96593648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261003-C-T

96593653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261008-A-G

96593713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261056-G-A

96593728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261071-G-T

96593838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261168-A-T

96593841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261171-A-G

http://identifiers.org/hco/10/GRCh38#96594653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41261869-A-C

96594664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261880-A-G

96594686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41261914-G-T

http://identifiers.org/hco/10/GRCh38#96595105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41262285-C-A

http://identifiers.org/hco/10/GRCh38#96595171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41262342-C-A

96595171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41262342-C-T

http://identifiers.org/hco/10/GRCh38#96595199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41262370-A-C

96595357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41262516-T-A

96595409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41262570-T-A

96595409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41262570-T-C

96595413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41262574-A-G

http://identifiers.org/hco/10/GRCh38#96595418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41262579-C-A

96595418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41262579-C-G

96595418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41262579-C-T

96595517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 41262674-T-A

96595517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 41262674-T-C

96595564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 41262722-T-G

96595572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41262730-T-C

96595753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41262912-A-G

96595753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41262912-A-T

96595784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41262939-C-T

96595871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41263016-A-G

96596341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41263737-C-T

96596375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41263767-T-G

96596444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41263842-G-A

96597181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41264658-T-C

96597255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41264816-T-G

96597343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41264953-C-T

96597345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41264955-T-C

96597345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41264955-T-G

96597367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41264976-T-C

96597403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41265011-C-T

http://identifiers.org/hco/10/GRCh38#96597408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41265016-A-C

96597415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41265024-T-C

96597632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41265192-T-G

96597714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41265250-G-T

96597773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41265323-C-T

96597822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41265360-C-T

96598320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41265872-G-T

96598548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41266018-G-A

http://identifiers.org/hco/10/GRCh38#96598623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41266527-C-A

96598623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41266527-C-T

96598720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41266618-G-A

96598834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41266715-G-A

96598872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41266743-A-G

96599374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41267178-C-T

96599507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41267309-A-G

96599731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41267497-G-A

96599963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41267890-C-T

96600248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41268197-A-G

96600929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41268609-G-A

96600983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41268657-T-C

96601076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41268733-G-A

96602264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270294-T-C

http://identifiers.org/hco/10/GRCh38#96602265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41270295-C-A

96602265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270295-C-G

96602265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270295-C-T

96602454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270503-G-T

http://identifiers.org/hco/10/GRCh38#96602480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41270529-C-A

96602480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270529-C-T

96602494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270541-G-A

96602494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270541-G-C

96602494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270541-G-T

http://identifiers.org/hco/10/GRCh38#96602536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41270576-C-A

96602536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41270576-C-T

http://identifiers.org/hco/10/GRCh38#96604121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41271661-C-A

96604121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41271661-C-T

96604152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41271692-T-A

96604152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41271692-T-C

96604607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41271851-A-G

96604632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41271876-A-T

96605280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41272303-G-A

96606224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41272446-C-T

96606309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41272527-C-T

96606313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41272531-C-T

96606381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41272596-T-G

96606439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41272651-A-G

96606617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41272816-T-C

96606987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41273038-A-T

96607177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41273208-A-G

http://identifiers.org/hco/10/GRCh38#96607687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41273674-A-C

96607734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41273728-G-A

96607790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41273766-C-G

96607827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41273805-T-G

96608087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274023-C-T

96608169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274114-G-A

96608254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274180-C-G

96608254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274180-C-T

96608260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274186-T-G

96608422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274336-G-T

96608653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274562-G-A

96608731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274677-C-T

96609027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41274966-C-T

96609356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275303-C-G

96609614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275746-A-G

http://identifiers.org/hco/10/GRCh38#96609626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41275756-C-A

96609626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275756-C-T

96609631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275761-A-T

http://identifiers.org/hco/10/GRCh38#96609664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41275785-C-A

96609664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275785-C-T

http://identifiers.org/hco/10/GRCh38#96609688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41275834-A-C

96609694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275860-G-A

96609694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275860-G-C

96609694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275860-G-T

http://identifiers.org/hco/10/GRCh38#96609695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41275861-C-A

96609695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41275861-C-T

http://identifiers.org/hco/10/GRCh38#96609696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41275862-A-C

96609806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41276003-T-A

96609806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41276003-T-C

96609979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276157-G-A

96609979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276157-G-T

http://identifiers.org/hco/10/GRCh38#96610016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41276182-C-A

96610016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276182-C-T

96610158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276313-C-T

96610236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276376-A-G

96610291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276459-G-T

96610299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276467-C-T

96610349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276515-A-G

96610430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276595-G-A

96610585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276752-G-A

96610610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276776-A-G

96610796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276947-A-G

96610796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41276947-A-T

96610882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41277019-C-T

96611110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41277238-G-A

96611446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41277560-T-C

96611448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41277562-T-C

96611959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41277783-A-G

96611987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41277811-T-C

http://identifiers.org/hco/10/GRCh38#96612180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41278005-C-A

96612180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41278005-C-T

96612181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41278006-G-A

96612269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41278085-C-G

96612348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41278155-G-A

96612375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41278166-T-G

http://identifiers.org/hco/10/GRCh38#96612526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41278324-C-A

96612567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41278522-A-G

http://identifiers.org/hco/10/GRCh38#96612574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41278529-C-A

96615388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41280187-G-A

96615558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41280336-G-T

96615658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41280426-A-G

96615667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41280435-C-T

96615761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41280519-G-A

96616330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41280858-G-A

http://identifiers.org/hco/10/GRCh38#96616370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41280891-A-C

96616399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41280907-A-G

96616506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281016-A-G

96616506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281016-A-T

96616516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281026-G-A

96616516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281026-G-T

96616534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281036-G-T

96616558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281060-A-G

http://identifiers.org/hco/10/GRCh38#96616572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41281074-A-C

96616572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281074-A-G

96616586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281088-C-T

96616594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281116-G-T

96616624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281177-T-C

96616668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41281221-C-T

96616721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281274-A-G

96616812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281364-C-T

96616814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281366-T-C

96616818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281370-A-G

96616819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281371-G-A

96616819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281371-G-T

http://identifiers.org/hco/10/GRCh38#96616823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41281375-C-A

96616823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281375-C-T

96617063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281593-C-T

96617102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281639-G-C

96617114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281647-C-T

96617151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281701-T-C

96617188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281748-T-A

96617196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281756-C-T

96617204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281765-G-T

96617338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281898-T-C

96617406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41281983-G-T

http://identifiers.org/hco/10/GRCh38#96617517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41282070-C-A

96617525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41282078-G-A

96617643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41282178-G-T

96617902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41282372-G-C

96617968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41282443-G-T

96618086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41282535-A-G

96618194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41282638-G-A

96618267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41282710-G-A

96618715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41283124-G-T

96619273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41283681-A-G

96619305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41283710-G-A

http://identifiers.org/hco/10/GRCh38#96619390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41283764-C-A

96619390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41283764-C-T

96619515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41283784-C-G

96619515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41283784-C-T

http://identifiers.org/hco/10/GRCh38#96619561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41283830-C-A

96619561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41283830-C-T

http://identifiers.org/hco/10/GRCh38#96619743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41284133-C-A

http://identifiers.org/hco/10/GRCh38#96620487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41284878-C-A

96620487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: synonymous variant
orthologous variants: 41284878-C-T

96620526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: synonymous variant
orthologous variants: 41284917-G-A

http://identifiers.org/hco/10/GRCh38#96620607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41284982-C-A

96620607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284982-C-G

96620607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284982-C-T

96620637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284986-G-A

96620637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284986-G-C

96620637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284986-G-T

96620638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284987-T-A

96620638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284987-T-C

96620650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41284999-G-T

96620665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285014-A-G

96620694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285047-G-A

96620694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285047-G-T

96620791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285141-A-G

http://identifiers.org/hco/10/GRCh38#96620793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41285143-A-C

96620793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285143-A-T

96621899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285645-G-A

96621899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285645-G-C

96622154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285848-C-T

96622295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41285975-C-T

96622705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286108-A-G

96622942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286339-A-G

96623107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286463-G-T

96623162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286519-G-C

96623181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286537-G-C

96623491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: synonymous variant
orthologous variants: 41286670-G-A

http://identifiers.org/hco/10/GRCh38#96623496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41286675-C-A

96623496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense variant
orthologous variants: 41286675-C-G

96623496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense variant
orthologous variants: 41286675-C-T

96623565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286762-T-A

96623565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286762-T-C

http://identifiers.org/hco/10/GRCh38#96623583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41286778-C-A

http://identifiers.org/hco/10/GRCh38#96623598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41286793-A-C

96623598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286793-A-G

http://identifiers.org/hco/10/GRCh38#96623615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41286825-C-A

96623615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286825-C-T

96623630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286840-T-A

96623630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286840-T-C

96623639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286849-G-A

96623639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41286849-G-T

http://identifiers.org/hco/10/GRCh38#96623703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41286894-A-C

96623889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41287785-C-G

http://identifiers.org/hco/10/GRCh38#96623917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41287813-A-C

96623929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41287826-G-A

http://identifiers.org/hco/10/GRCh38#96623989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41287882-A-C

96624004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41287897-G-C

96624083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41287948-C-G

96624254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41288109-T-C

96624263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41288118-T-C

96624363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41288214-G-A

96624470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41288317-A-G

96624594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41288636-G-A

96626418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41290564-T-C

http://identifiers.org/hco/10/GRCh38#96626584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41290721-C-A

96626584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41290721-C-T

http://identifiers.org/hco/10/GRCh38#96626595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41290732-C-A

http://identifiers.org/hco/10/GRCh38#96626646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41290780-C-A

96626646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41290780-C-T

96626675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41290809-A-G

96626688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41290842-T-C

96626778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: synonymous variant
orthologous variants: 41290932-T-C

96626850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: synonymous_variant, undefined
orthologous variants: 41291001-T-C

96626850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense_variant, undefined
orthologous variants: 41291001-T-G

http://identifiers.org/hco/10/GRCh38#96626946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41291101-C-A

96626975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41291130-G-T

96626978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41291133-T-A

96626978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41291133-T-C

http://identifiers.org/hco/10/GRCh38#96627035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41291186-A-C

http://identifiers.org/hco/10/GRCh38#96627042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41291192-C-A

96627481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41295695-T-C

96627520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41295722-C-T

96627527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41295729-C-G

96627639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41296131-C-G

96627692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41296181-G-C

96627790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41296302-G-A

96627834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41296369-C-T

http://identifiers.org/hco/10/GRCh38#96627868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41296403-C-A

96628038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41296565-A-G

96628057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41296584-A-T

96628295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41296822-A-G

96629171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41297436-T-C

96629374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41297616-G-A

96629395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41297637-A-T

http://identifiers.org/hco/10/GRCh38#96633005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41299491-A-C

96633100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41299594-G-A

96633100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41299594-G-C

96633100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41299594-G-T

96633233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41299724-G-A

96633233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41299724-G-T

96633239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41299730-T-C

96633272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41299763-G-A

96633380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41299870-G-C

96633380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41299870-G-T

96633453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41299941-A-G

96633577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41300045-A-G

96634110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302295-G-A

96634110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302295-G-C

96634179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302344-C-T

96634487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302622-G-A

96634496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302631-C-G

96634660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302795-C-T

96634737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302853-C-G

96634737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41302853-C-T

http://identifiers.org/hco/10/GRCh38#96634903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41302989-A-C

96635032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303093-C-T

96635064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303125-T-C

96635067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303128-G-C

http://identifiers.org/hco/10/GRCh38#96635096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41303157-C-A

96635096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303157-C-T

96635326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303349-C-T

96636608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303678-C-T

96636777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303828-G-A

96636892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41303943-G-A

96637074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304116-A-G

96637132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304176-C-G

96637294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304324-G-T

96638522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304359-C-T

96638627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304440-C-T

96638650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304460-C-T

96639077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304762-A-G

96639152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304836-G-C

96639156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304840-T-C

96639156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304840-T-G

96639168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304851-G-A

96639195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304877-C-G

96639209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304900-G-T

96639283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41304984-G-A

96639374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305064-C-T

http://identifiers.org/hco/10/GRCh38#96639516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41305212-A-C

96639750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305384-G-C

96639956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305573-T-A

96640071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305692-G-A

96640090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305711-G-A

96640140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305762-A-G

96640176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305796-A-G

96640193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41305806-C-G

http://identifiers.org/hco/10/GRCh38#96640368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41305973-C-A

96640562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306122-G-C

96641004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306220-G-A

96641024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306240-T-C

96641038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306255-G-A

96641114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306330-T-C

96641115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306331-G-A

96641115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306331-G-T

96641120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306336-T-C

96641128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306349-T-C

96641140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306361-C-T

96641152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41306373-C-T

96641427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306606-T-C

96641428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306607-G-A

96641500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306665-C-T

96641580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306753-T-C

http://identifiers.org/hco/10/GRCh38#96641582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41306755-C-A

96641629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306800-G-A

96641695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306864-T-A

96641765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41306933-T-C

96641886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41307090-G-A

96641960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41307159-C-T

96642724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41307522-G-T

http://identifiers.org/hco/10/GRCh38#96642831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41307572-A-C

96642851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41307589-G-A

96643208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308188-G-A

96643250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308229-C-G

96643441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308379-G-A

96643754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308559-C-G

96643776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308581-G-A

96643807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308613-G-A

96643956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308743-C-T

96643988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308775-G-A

96644127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41308840-C-G

96644903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41309367-C-T

96644962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41309433-G-A

96645121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41309613-T-C

96645130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41309622-C-T

http://identifiers.org/hco/10/GRCh38#96645411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41309879-C-A

96645411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41309879-C-T

http://identifiers.org/hco/10/GRCh38#96645491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41309959-C-A

96645491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41309959-C-G

96645525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41309993-C-G

96645528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41309996-G-A

96645528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41309996-G-C

96645591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41310059-G-A

96645591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 41310059-G-C

96645597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41310065-A-G

http://identifiers.org/hco/10/GRCh38#96645657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41310125-C-A

96645657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41310125-C-T

96645680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310147-G-T

http://identifiers.org/hco/10/GRCh38#96645805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41310271-C-A

96645969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310380-C-T

http://identifiers.org/hco/10/GRCh38#96645973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41310384-C-A

96646282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310386-G-A

96646293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310397-T-G

96646340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310445-G-A

96646352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310457-A-G

96646453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310530-C-T

96646597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310633-G-T

96646622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310652-T-G

96646693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310715-G-A

96646870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310883-C-T

96646930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310942-T-A

96646989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41310988-C-G

96647202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41311417-A-G

96647257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41311472-T-C

96647449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41311645-C-T

96647505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41311701-T-C

96647845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41312020-G-C

96648396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41312486-T-C

96648472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41312767-C-T

96648517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41312782-A-T

96648620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41312885-T-C

http://identifiers.org/hco/10/GRCh38#96648902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41313168-A-C

96648902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313168-A-G

96648926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313172-T-C

96648926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313172-T-G

96648946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313193-T-A

96648946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313193-T-C

96648946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313193-T-G

96648978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313225-G-C

96648978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313225-G-T

96648979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313226-A-G

96648979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313226-A-T

96648986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41313233-G-A

96650046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41314962-A-G

96650078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41314994-C-T

http://identifiers.org/hco/10/GRCh38#96650101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41315017-A-C

http://identifiers.org/hco/10/GRCh38#96650215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41315129-C-A

96650305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41315211-G-C

96650408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41315287-C-T

96650412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41315290-C-T

96650913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41315780-T-A

96651237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316259-T-C

96651351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41316373-C-G

96651400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316422-T-C

96651424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316446-C-G

96651425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316447-T-C

96651428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316450-C-T

96651485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316507-C-T

96651488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316510-G-A

96651504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316526-C-T

96651608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41316630-G-A

http://identifiers.org/hco/10/GRCh38#96651638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41316660-C-A

96651638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41316660-C-T

http://identifiers.org/hco/10/GRCh38#96651697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41316717-C-A

96651854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41316861-G-A

96652065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317282-C-T

96652685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317626-G-A

96652879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317821-T-C

96652920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317861-T-A

96652920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317861-T-C

96652946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317890-G-A

96652965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317907-G-A

96652965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41317907-G-T

96654350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41319011-C-T

96656521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320394-G-A

96656625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320493-G-T

96656702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320552-G-A

96656702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320552-G-T

http://identifiers.org/hco/10/GRCh38#96656851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41320701-C-A

96656851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41320701-C-G

96656851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41320701-C-T

96656953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320803-C-T

96656993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320844-T-A

96657033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320884-G-A

96657033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320884-G-T

96657144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41320985-C-T

96657409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41321141-G-T

96657469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41321200-C-T

96663825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41324350-T-C

96663868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41324387-T-C

http://identifiers.org/hco/10/GRCh38#96664153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41324758-A-C

96664298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325050-C-T

http://identifiers.org/hco/10/GRCh38#96664389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41325159-C-A

96664389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325159-C-T

96664427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325242-T-C

96664437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325252-G-A

96664586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325289-C-T

96664865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325518-A-G

96664868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325521-G-A

http://identifiers.org/hco/10/GRCh38#96664949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41325590-C-A

96665036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325672-C-T

96665073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41325706-C-T

96665448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41326734-C-T

96665523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41326798-G-A

96665975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327144-C-T

http://identifiers.org/hco/10/GRCh38#96666194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41327352-A-C

96666194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327352-A-T

96666195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327353-G-A

96666442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327520-T-A

96666442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327520-T-G

96666450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327528-G-A

96666571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327591-A-G

96666727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327720-A-G

96666782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327771-A-G

96666792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41327781-T-C

96667336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41328266-T-C

96667560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41328477-A-G

http://identifiers.org/hco/10/GRCh38#96667848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41329220-C-A

96668007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41329371-A-G

96668036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41329399-C-T

96668607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41330269-A-G

96668613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41330273-A-G

96670583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41330962-C-T

96670591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41330970-A-G

96671013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41331444-T-C

96671273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41331675-T-C

96671363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41331761-C-T

96672907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333047-C-T

96672946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333111-T-A

http://identifiers.org/hco/10/GRCh38#96672988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41333146-C-A

96673194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333302-C-T

96673281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333387-G-A

96673420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333500-C-T

96673484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333564-A-G

96673591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333681-G-A

96673750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333838-G-C

96674134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41334428-A-G

96674186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41334564-C-T

96675722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41335650-C-T

96675800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41335725-T-G

96676109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336022-G-A

96676304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336200-C-T

http://identifiers.org/hco/10/GRCh38#96676339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41336314-C-A

96676577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336703-A-T

96676673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336800-G-A

96676673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336800-G-T

96676674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336801-A-G

96676674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336801-A-T

96676795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41336933-C-G

96676924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41337027-C-G

96677147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41337215-G-A

96677282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41337337-C-T

96677762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41337795-G-C

96679175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41338544-A-G

http://identifiers.org/hco/10/GRCh38#96680863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41339068-C-A

96681066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41339271-G-A

96681240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41339400-G-A

96681560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41339674-G-A

96681631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41339746-G-A

96681689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41339802-A-G

96681770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41339852-T-C

96681821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41339900-G-A

http://identifiers.org/hco/10/GRCh38#96681931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41340030-A-C

96681961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41340056-T-C

96682196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41340251-G-A

96682464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41340496-C-G

96682855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41340883-A-G

96683289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41341360-T-C

96683369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41341396-C-G

96683371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41341398-A-G

96683467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41341474-T-G

96683704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41341674-T-C

96683883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41341874-A-G

96684139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41342083-A-T

96684232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41342169-T-C

http://identifiers.org/hco/10/GRCh38#96684261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41342198-A-C

96684306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41342243-A-G

96684566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41342461-C-G

96684566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41342461-C-T

96684758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41342620-G-A

96684863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41342706-T-C

96685282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343124-T-C

96685284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343126-G-A

96685375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343180-G-A

96685865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343564-C-T

96685876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343584-C-T

96685925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343632-C-G

96685937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343644-T-C

96686013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343714-G-A

96686057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343762-G-A

96686126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343828-C-G

96686132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343834-A-G

96686206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343905-T-A

96686206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343905-T-C

96686284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41343955-A-G

http://identifiers.org/hco/10/GRCh38#96686342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41344014-C-A

96686391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41344061-G-A

96686391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41344061-G-C

96686633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41344659-T-G

http://identifiers.org/hco/10/GRCh38#96686704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41344731-A-C

96686743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41344772-T-C

96686769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41344797-C-T

96687356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41345029-G-A

96687360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41345033-C-T

http://identifiers.org/hco/10/GRCh38#96687587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41345246-C-A

96687587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41345246-C-T

96688019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41345783-C-T

96688181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41345930-C-T

96688256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41346004-C-T

96688527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41346269-G-A

96690837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41347512-G-C

96690895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41347569-T-G

96690944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41347623-T-C

96691066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41347719-G-A

96691151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41347797-T-C

96691356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41347988-G-A

96693275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41351724-C-T

96693350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41351820-C-T

96693351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41351821-G-A

96693351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41351821-G-T

96693577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41352182-T-A

96694350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353233-A-G

96694368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353247-C-T

96694439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353306-T-C

96694452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353319-C-T

96695121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353622-T-G

96695137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353627-T-C

96695358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354000-C-G

96695876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354531-T-G

96695945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354594-C-T

96696077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354726-A-G

96696458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355086-A-T

96696477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355105-C-G

96696477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355105-C-T

96696608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355231-C-T

96696708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355361-T-C

96696776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355423-A-G

96697001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355650-A-G

96697027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355673-T-C

96697244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355882-A-G

96697814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356158-C-T

96698074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356443-G-T

96698130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356503-T-C

96698191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356563-G-A

96699606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357236-G-A

96699606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357236-G-C

96700173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357770-A-G

96700204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357802-G-A

96700240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357839-C-T

96700306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41357930-G-A

96700311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41357935-A-G

96700361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357985-C-T

96700616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41358241-A-T

http://identifiers.org/hco/10/GRCh38#96700703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41358321-C-A

96700757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41358377-G-T

http://identifiers.org/hco/10/GRCh38#96700923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41358521-C-A

96700980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: 41358559-T-C

96701234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41358795-G-T

96701235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41358796-C-T

96701265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41358825-G-A

96701265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41358825-G-C

96701648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41359399-G-A

96702111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41359908-T-C

96703368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41360745-G-A

96703581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41360947-T-C

96703739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41361111-G-A

http://identifiers.org/hco/10/GRCh38#96703892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41361255-C-A

96704001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41361353-C-T

96704085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41361445-C-T

96704133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41361494-C-T

96704178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41361530-C-T

96704278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41361627-G-A

96707004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41361902-C-T

96707140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362033-A-G

96707160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362049-A-T

96707230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362118-A-G

96707384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362209-C-G

96707661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362464-T-C

http://identifiers.org/hco/10/GRCh38#96707826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41362630-A-C

96707863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362661-T-C

96707985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362781-G-A

96707985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362781-G-C

96707988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41362784-A-G

http://identifiers.org/hco/10/GRCh38#96708093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41363424-C-A

96708126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41363458-G-A

96708626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41363644-G-A

96708641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: 41363659-G-A

96708641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: 41363659-G-T

96708750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41363774-T-C

96709211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41363907-G-A

96709258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41363954-T-C

96709466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364173-A-T

96709487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364194-A-G

http://identifiers.org/hco/10/GRCh38#96709525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41364239-C-A

96709525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364239-C-T

96709592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 41364310-T-C

96709627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 41364345-G-C

http://identifiers.org/hco/10/GRCh38#96709859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41364580-C-A

96709872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 41364593-A-G

96709894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 41364615-G-A

96709894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 41364615-G-T

96709946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 41364667-G-A

96709967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 41364688-G-A

96709974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 41364695-C-G

96709974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 41364695-C-T

96710014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364731-A-G

http://identifiers.org/hco/10/GRCh38#96710025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41364749-C-A

96710025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364749-C-G

96710037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364761-C-T

http://identifiers.org/hco/10/GRCh38#96710072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41364792-C-A

96710262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364939-A-G

96710262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41364939-A-T

96710884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41365405-T-C

96710973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41365474-G-A

96711101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41365532-G-A

http://identifiers.org/hco/10/GRCh38#96711128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41365562-A-C

96711338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41365778-G-C

96711405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41365844-T-G

96711466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41365920-G-A

96711548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41366185-G-T

96711603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41366238-T-C

96716458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41370047-C-T

96716770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41370313-A-G

96716803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41370345-G-T

96717650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41370810-G-A

96717650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41370810-G-C

96717937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371035-C-G

96717986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371069-G-A

96718238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371371-T-C

96718246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371379-A-G

96718250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371384-T-C

96718404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371530-C-G

96718758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371819-C-T

96718780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371842-C-T

http://identifiers.org/hco/10/GRCh38#96718781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41371843-A-C

96718920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41371974-G-A

96719050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372130-C-G

96719143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372207-T-G

96719165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372229-A-G

96719206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372279-C-T

96719254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372312-C-G

96719294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372358-C-G

96719342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: 41372399-T-G

96719453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372505-T-A

96719575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41372624-C-T

96719900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: 41372932-A-G

96720033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: 41373034-G-A

http://identifiers.org/hco/10/GRCh38#96720053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41373055-C-A

96720208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron_variant, undefined
orthologous variants: 41373201-G-A

http://identifiers.org/hco/10/GRCh38#96720280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41373273-C-A

96720280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41373273-C-T

http://identifiers.org/hco/10/GRCh38#96720346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41373363-C-A

96720346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41373363-C-G

96720346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41373363-C-T

96720366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41373381-G-A

96720366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: intron variant
orthologous variants: 41373381-G-T

http://identifiers.org/hco/10/GRCh38#96720434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41373458-C-A

96720434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373458-C-T

96720442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373466-G-A

96720442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373466-G-C

96720442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373466-G-T

http://identifiers.org/hco/10/GRCh38#96720453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41373478-C-A

96720453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373478-C-G

96720453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373478-C-T

http://identifiers.org/hco/10/GRCh38#96720456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41373481-C-A

96720456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373481-C-T

96720477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373505-A-T

96720480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: 41373508-G-A

http://identifiers.org/hco/10/GRCh38#96720509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41373536-C-A