96248820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25581230-T-G

96248879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25581164-A-G

http://identifiers.org/hco/6/GRCh38#96248920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25581123-C-A

96249096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25581021-G-A

96249190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25580930-T-C

96249266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25580858-G-A

96249648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25574069-G-A

96249689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25573992-C-T

96249721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25573962-T-C

96249792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25573895-T-C

96250343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25573395-A-T

96250411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25573327-A-G

96250421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25573317-G-A

96250511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25573234-T-G

96250852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25572840-T-C

http://identifiers.org/hco/6/GRCh38#96251076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25572617-A-C

96251216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25572494-T-C

96251335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25572371-A-T

96257409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553013-A-G

http://identifiers.org/hco/6/GRCh38#96257443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25552974-C-A

96258247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25551318-G-A

96258326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25551247-C-T

96258433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25551150-G-A

96258567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25551037-C-T

96258611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25551021-A-G

96258660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550975-C-T

96258732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550907-C-G

96258947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550714-G-T

http://identifiers.org/hco/6/GRCh38#96258951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25550710-C-A

96258951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550710-C-G

96258951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550710-C-T

http://identifiers.org/hco/6/GRCh38#96258988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25550685-A-C

96259179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550546-A-G

96259283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550438-T-A

96278678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25533593-C-T

96278751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25533516-C-T

96278851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25533429-T-C

96279196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25533111-A-G

96279336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25532972-A-G

96279375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25532933-T-G

96283264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25526184-A-G

96283420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25526042-A-G

96283465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25526012-G-T

96283466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25526011-A-T

96283468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25526009-A-G

96284027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25525514-T-C

96284268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25525207-G-C

96284334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25525168-C-T

http://identifiers.org/hco/6/GRCh38#96284487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25525011-A-C

96284505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524993-A-T

96284774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524740-A-T

96285613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524684-A-G

96285614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524683-A-G

96285688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524611-G-T

96285755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524544-A-G

96285757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524542-T-G

96285853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524454-A-G

http://identifiers.org/hco/6/GRCh38#96286187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25524180-A-C

96286199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524168-G-A

96286199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524168-G-T

96302996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25511227-G-T

96303100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25511122-T-A

96303100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25511122-T-C

96303309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510930-G-A

96303398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510829-C-T

96303497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510735-C-T

96303644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510457-C-T

96303653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510448-G-A

96303721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510376-T-C

96303756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510340-T-A

96304004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510102-A-T

96304192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509975-G-T

96304209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509958-T-C

96304285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509904-A-G

96304285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509904-A-T

96304354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509838-A-G

http://identifiers.org/hco/6/GRCh38#96304440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25509759-C-A

96304440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509759-C-T

96304458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509740-A-G

96304499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509704-G-T

96319925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478066-C-T

96320287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477898-A-G

96320357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477818-T-C

96320395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477786-A-T

96320528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477656-A-T

96320573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25477614-T-G

http://identifiers.org/hco/6/GRCh38#96320916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25477334-A-C

96325010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467377-C-G

http://identifiers.org/hco/6/GRCh38#96325037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25467351-A-C

96325049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467339-T-A

96325049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467339-T-C

96325215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467186-T-A

96325675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466781-A-G

96325740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466713-A-T

http://identifiers.org/hco/6/GRCh38#96325997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25466515-C-A

96329083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465086-C-T

http://identifiers.org/hco/6/GRCh38#96329161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25465008-C-A

96329370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464799-T-A

96329703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464619-A-G

http://identifiers.org/hco/6/GRCh38#96329725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25464598-C-A

96329725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464598-C-T

96329859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25464525-T-C

96329894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25464489-G-C

http://identifiers.org/hco/6/GRCh38#96330076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25464311-A-C

96330168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464208-A-G

96330254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464168-T-C

96330334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464110-G-A

96330350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464101-A-G

96330350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464101-A-T

96330730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463763-T-C

96330978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463573-T-A

96331035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463519-T-C

96331117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463439-G-A

96331117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463439-G-T

96331119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463437-C-T

96331279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463299-A-G

96331297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463285-G-A

96331900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462734-A-G

96331902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462732-A-T

96332007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462634-T-C

96332345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462317-A-G

96350868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458624-G-C

96350913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458578-C-T

96350960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458488-T-C

96351056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458394-G-A

96351173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458280-T-C

96351584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454885-A-T

96351730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455015-G-C

96351896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455332-A-G

96351966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455388-C-T

96352022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455420-C-T

96352081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455478-C-T

96352241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455616-A-G

96352265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455640-G-T

http://identifiers.org/hco/6/GRCh38#96352307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25455693-A-C

96352491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454647-T-G

http://identifiers.org/hco/6/GRCh38#96352501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25454637-C-A

96352594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454553-T-C

http://identifiers.org/hco/6/GRCh38#96352713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25454435-A-C

96352954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454218-G-C

96353035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454148-G-A

96353144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454034-C-T

http://identifiers.org/hco/6/GRCh38#96353205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25453974-A-C

96353398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453816-C-T

96355905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453037-A-G

96355969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25452977-G-C

96356001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25452947-T-C

96368343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445903-T-C

96368392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445853-A-G

96368505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445007-T-C

96369117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444428-T-C

96369378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444214-T-C

96369610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444006-T-C

96369630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443986-T-A

96369768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443868-A-G

96369769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443867-T-C

96369900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443752-G-A

96369936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443717-T-C

96370246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443407-C-T

96371876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441915-T-C

96372318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25436395-G-A

96372708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25433759-T-A

96377417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426995-A-G

96377546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426864-C-G

96378202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424992-T-C

96378225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424973-C-T

96378334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424838-G-A

96378334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424838-G-T

96378856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424069-G-A

96379042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423879-G-A

96379042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423879-G-T

96379088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423834-G-C

96379366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423566-G-A

96379366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423566-G-C

96379634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423298-A-G

96379634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423298-A-T

96379667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423276-G-A

http://identifiers.org/hco/6/GRCh38#96382871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25421495-A-C

96382888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421462-T-C

96382988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421355-G-T

96383050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421300-A-T

96383278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420939-C-T

96383551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420662-G-C

96383575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420637-G-A

96383589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420623-G-C

96384700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418184-T-A

96384717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418167-C-T

96384735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418149-A-T

96384966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417897-G-T

96385015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417846-A-G

96385027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417834-T-C

96385054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417818-T-C

96385062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417810-G-A

96385129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417744-T-C

96386566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415760-G-A

http://identifiers.org/hco/6/GRCh38#96386570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25415756-A-C

96386789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415530-A-G

96387460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25414112-T-C

96389856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25412195-A-G

96390017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25412042-T-A

96390029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25412030-G-A

96390221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25411842-C-T

96390404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25411654-A-G

96390471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25411592-T-C

96390840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25410815-T-C

96390981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25410694-G-A

96391063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410623-G-A

96391278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409590-G-A

96391326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409500-C-T

96391729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409110-T-C

96391729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409110-T-G

96391915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408932-G-A

96392100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408744-T-C

http://identifiers.org/hco/6/GRCh38#96392729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25408107-C-A

96392798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408037-T-C

96392816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408016-G-A

96392828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408004-T-C

96393604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407228-T-C

96393631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407199-T-C

96393710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407166-T-C

96393796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407085-G-A

96393830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407048-G-A

96393853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407028-G-T

96393952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25405687-T-C

96394324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25405628-T-G

96394373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25405570-A-T

96394599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25405047-T-C

96394605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25405041-A-T

http://identifiers.org/hco/6/GRCh38#96394722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25404956-A-C

96394796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404884-C-G

96394930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404800-T-C

96395165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404596-G-A

96400473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25401441-A-T

96400677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25401249-T-C

http://identifiers.org/hco/6/GRCh38#96400742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25401184-A-C

96400835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25401091-T-C

96400841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25401086-A-G

96400935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400999-T-C

96402631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25393943-G-A

96402891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25393645-T-G

96403130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25393389-C-G

96403146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25393372-T-C

96410371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25392509-G-A

96410591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25392331-A-G

96410632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25392289-C-T

96410688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25392234-A-G

96410964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25391942-A-G

96411387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25391239-T-C

96411419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25391205-C-G

96411419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25391205-C-T

http://identifiers.org/hco/6/GRCh38#96411509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25391124-C-A

96411691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25390999-A-T

96412121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25390749-G-A

96412215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25390686-C-G

96412384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25390515-G-A

96412427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25390476-A-G

96412533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25390375-T-A

96412591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25390312-G-A

96413112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389812-A-G

96413283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389644-T-C

96413435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389516-T-C

96413499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389463-T-C

http://identifiers.org/hco/6/GRCh38#96413640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25389015-C-A

96413640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389015-C-T

96413705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388950-A-G

96414173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388475-C-T

http://identifiers.org/hco/6/GRCh38#96417776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25376510-A-C

96418296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25374841-T-C

96418660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25374479-T-C

http://identifiers.org/hco/6/GRCh38#96419205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25370989-C-A

96419783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25370427-G-C

96419806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25370416-A-G

96420221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369698-T-C

96420341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369578-G-A

96420341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369578-G-T

96420395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369545-A-T

96420470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369502-C-T

96421229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369151-T-C

96421273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369087-C-T

96421359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25369001-C-T

http://identifiers.org/hco/6/GRCh38#96421700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25368659-A-C

96445836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

96445836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

96445970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

96446498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

96446498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

96446655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/6/GRCh38#96446700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

96446740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96446944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

96446946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

96446946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

96446949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

96447074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

96447074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

96447075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

96447229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

96447379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

http://identifiers.org/hco/6/GRCh38#96447441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

http://identifiers.org/hco/6/GRCh38#96447450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

96447478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

96447503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

96447707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

96447708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

96447952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

96448035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

96448132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

96448264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

96448469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96448804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

96448882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96448990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

96449899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

96449960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

96449960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

96449990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96450157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

96450335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96450410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

http://identifiers.org/hco/6/GRCh38#96450423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

96450634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

96450678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

96450923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

96450963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96451069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96451265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

96462721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25347199-G-A

96462887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25347033-A-T

96462938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346983-C-T

http://identifiers.org/hco/6/GRCh38#96463132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25346780-C-A

96463180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346754-A-G

96463180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346754-A-T

96463192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346742-A-G

96463570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346374-T-C

96463570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346374-T-G

96463615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346330-G-C

96463618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25346327-C-T

96464185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345751-C-T

96464272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345689-C-T

96464690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345263-G-C

96464695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345250-G-A

96465145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25344822-T-C

http://identifiers.org/hco/6/GRCh38#96465454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25344617-A-C

96465967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25344190-T-C

96466469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25341401-T-C

96466517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25341359-T-C

96466544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25341332-T-C

96466614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25341262-C-T

96466864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25340968-A-T

96466985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25340841-G-A

96467032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25340794-C-G

96467062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25340764-T-C

http://identifiers.org/hco/6/GRCh38#96467182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25340647-A-C

http://identifiers.org/hco/6/GRCh38#96467365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25340469-A-C

96467663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25339188-G-T

96467767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25339094-C-T

96467771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25339090-T-G

http://identifiers.org/hco/6/GRCh38#96467863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25339004-C-A

96467863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25339004-C-G

96467863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25339004-C-T

96467875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25338992-C-T

96467876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25338991-A-T

96468139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25338761-A-G

96468481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25338430-A-G

96468481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25338430-A-T

96468656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25338265-G-A

96468898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25338076-C-T

96468992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25337983-A-G

96469106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25337858-G-A

96469106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25337858-G-T

96469844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25336873-C-T

96469858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25336859-C-T

96470405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25334041-T-C

http://identifiers.org/hco/6/GRCh38#96470958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25329155-C-A

96470958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329155-C-T

96470960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329157-C-T

96470964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329161-C-T

96471201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329329-G-C

96471323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329928-A-G

96471330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329935-G-T

96471398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330003-A-G

96471722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330344-A-G

96471873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330482-T-C

96471891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330500-T-C

96472030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330610-A-G

96479461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330732-T-A

96479509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330783-T-A

96479671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330945-G-A

96479933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25331631-T-C

96479954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25331653-T-A

96480199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25332536-C-T

96480487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333066-A-G

96480517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333096-A-G

96480725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333307-G-T

96507217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307651-T-C

96507315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307565-T-C

96507343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307533-G-A

96507654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307224-C-T

96507684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307197-T-C

96507737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307140-A-G

96507745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307132-C-T

96507820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25307064-T-C

96507896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25306994-T-C

96511073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25306033-T-G

96511560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25305623-T-C

96511610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25305571-C-T

96511673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25305495-C-T

96511825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25305345-T-A

96511984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25304870-C-T

96512178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25304293-A-G

http://identifiers.org/hco/6/GRCh38#96512436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25304139-A-C

96512531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25304037-T-C

96512549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25304019-A-G

96512804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25303397-A-G

96512822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25303381-A-G

96513024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25303221-C-T

96513049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25303194-T-C

96513132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25303118-C-G

96513346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25302885-G-A

96513476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25302770-A-G

http://identifiers.org/hco/6/GRCh38#96513558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25302689-A-C

http://identifiers.org/hco/6/GRCh38#96513633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25302632-A-C

96513691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25302567-A-G

96513839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25302099-G-C

http://identifiers.org/hco/6/GRCh38#96513845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25302093-C-A

96513906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25302030-A-G

96513950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25301971-T-C

96514166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25301830-T-C

96515649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25287494-T-C

96515844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25287317-G-T

96515933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25287235-T-C

96516006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25287157-G-C

http://identifiers.org/hco/6/GRCh38#96516021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25287146-A-C

96516227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25286968-C-T

96518031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25283077-G-A

96518165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25282946-T-C