168915437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3 prime UTR variant
orthologous variants: 69064533-A-G

168915560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3 prime UTR variant
orthologous variants: 69064630-G-A

168916006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69065003-A-T

168916323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69065391-T-C

168916955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69066053-G-T

168916993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69066369-C-G

168921014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69066969-T-A

168921014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69066969-T-C

168921034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69066982-C-T

168921517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69067455-T-C

168921755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69067673-G-A

168922015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69067895-A-T

168922056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69067932-A-G

168922292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068197-C-T

168922305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068209-C-T

168922310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068214-A-T

168922312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068216-T-C

168922474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068376-C-T

168922483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068385-A-G

168922488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068390-C-T

168922633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068537-A-G

168922936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068806-G-T

168922984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068833-A-G

http://identifiers.org/hco/2/GRCh38#168922994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69068843-C-A

168922997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068846-G-T

168923030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068881-C-T

168923110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69068984-T-C

168923146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69069019-T-C

http://identifiers.org/hco/2/GRCh38#168923380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69069225-C-A

168923380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69069225-C-G

168923380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69069225-C-T

168923486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69069325-C-G

168923652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 69069458-T-A

168923664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 69069470-T-C

168923697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 69069503-C-T

168923760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 69069566-G-A

168923849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69069656-G-A

168923849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69069656-G-C

168923849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69069656-G-T

168923920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69069723-A-G

168924081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69069862-T-A

168924081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69069862-T-C

http://identifiers.org/hco/2/GRCh38#168924130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69069909-A-C

168924228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070003-A-G

168924249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070021-C-T

168924266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070038-A-G

168924308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070079-A-G

168924308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070079-A-T

http://identifiers.org/hco/2/GRCh38#168924445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69070288-C-A

168924445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070288-C-T

168924469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070331-A-T

168924472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070334-T-A

168924514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070372-T-A

168924514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070372-T-C

168924516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070374-G-T

168924558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070414-G-A

168924558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070414-G-C

168924558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070414-G-T

168924575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070432-A-G

168924594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070450-G-A

168924594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69070450-G-T

168924848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69073949-C-T

168925309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69074399-T-A

168925416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69074527-T-C

168925654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69074929-C-T

168925666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69074941-C-T

168925962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69075198-T-A

168925995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69075232-G-T

168926020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69075257-T-C

168926044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69075289-C-G

168926044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69075289-C-T

http://identifiers.org/hco/2/GRCh38#168926234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69075472-C-A

168926289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69075525-G-A

168926311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69075549-G-A

168927089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076018-C-T

168927091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076020-C-T

168927210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69076143-G-C

168927327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 69076260-G-A

168927380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076315-G-A

168927380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076315-G-T

168927384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076319-G-A

168927441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076375-G-A

168927441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076375-G-T

168927471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076389-A-T

168927473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076391-T-A

168927473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076391-T-C

168927473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076391-T-G

168927575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076491-T-C

168927707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076638-A-G

168927903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69076854-C-T

168928105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077258-T-A

168928189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077347-A-G

168928364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077519-C-T

168928446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077591-T-C

168928610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077743-A-G

168928728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077853-C-T

168928748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077874-T-C

168928775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077901-T-C

168928798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077923-A-G

168928816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69077941-T-C

168930074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078475-T-G

168930085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078486-T-A

168930144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078553-G-T

168930264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078658-T-A

168930264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078658-T-C

http://identifiers.org/hco/2/GRCh38#168930521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69078912-C-A

168930521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078912-C-T

168930523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078914-G-A

168930523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078914-G-C

168930536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078925-A-G

168930555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078945-T-C

168930555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078945-T-G

http://identifiers.org/hco/2/GRCh38#168930563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69078953-C-A

168930563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078953-C-T

168930595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078984-T-A

168930597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078986-A-G

http://identifiers.org/hco/2/GRCh38#168930602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69078991-C-A

168930602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69078991-C-T

168930649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079042-A-G

168930650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079043-G-A

168930650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079043-G-C

168930650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079043-G-T

168930657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 69079050-T-C

http://identifiers.org/hco/2/GRCh38#168930665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69079058-C-A

168930665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 69079058-C-T

168930669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69079062-T-C

http://identifiers.org/hco/2/GRCh38#168930679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69079072-C-A

168930680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079073-A-G

168930680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079073-A-T

168930695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079088-T-C

168930707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079100-A-G

168930725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079118-A-G

168930776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079169-T-C

168930776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079169-T-G

168930779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079172-G-A

168930779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079172-G-C

http://identifiers.org/hco/2/GRCh38#168930797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69079190-C-A

168930797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69079190-C-T

168930881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079274-A-G

168930894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079287-T-C

168930908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079301-A-G

168931066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69079585-C-T

168931856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69087383-T-C

168931883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69087410-A-G

http://identifiers.org/hco/2/GRCh38#168932497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69087671-A-C

168932575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69087753-G-A

168932584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69087762-G-C

168932703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69087848-T-G

http://identifiers.org/hco/2/GRCh38#168933266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69088099-A-C

168933289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69088122-T-G

168933309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69088142-T-C

168933504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69088329-C-G

168934256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089044-G-A

http://identifiers.org/hco/2/GRCh38#168934414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69089150-A-C

168934523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089204-G-A

168934523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089204-G-T

168934602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089276-C-T

168934607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089281-G-C

168934815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089473-A-G

168935039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089673-A-G

168935039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089673-A-T

168935040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089674-G-A

http://identifiers.org/hco/2/GRCh38#168935126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69089751-C-A

168935126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089751-C-T

168935135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089773-T-C

168935138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089776-T-C

168935143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089781-T-C

168935181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69089824-C-T

168935186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 69089829-G-C

http://identifiers.org/hco/2/GRCh38#168935261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69089904-A-C

168935460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69090101-G-T

168935488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69090129-A-G

168935489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69090130-G-A

168935489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69090130-G-C

168935498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69090139-T-A

http://identifiers.org/hco/2/GRCh38#168935702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69091277-C-A

168935765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69091352-C-G

168936177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69091657-G-T

168936249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 69091726-G-A

168936354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_acceptor_variant, undefined
orthologous variants: 69091831-C-T

168936504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69091982-G-A

168936504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69091982-G-C

168936504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69091982-G-T

168936532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69092022-A-G

168936536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69092026-T-A

168936536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69092026-T-C

168936537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69092027-A-G

http://identifiers.org/hco/2/GRCh38#168936553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69092043-C-A

168936553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69092043-C-T

http://identifiers.org/hco/2/GRCh38#168936566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69092056-C-A

http://identifiers.org/hco/2/GRCh38#168936581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69092071-C-A

168936623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69092139-C-T

168936668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69092184-A-G

168936725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69092234-C-T

http://identifiers.org/hco/2/GRCh38#168936750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69092258-C-A

168936803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69092312-C-T

168943533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69094390-T-C

168943614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69094470-G-A

168943614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69094470-G-T

168943692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69094539-G-A

168943955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69094698-A-G

http://identifiers.org/hco/2/GRCh38#168944149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69095039-A-C

168944187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69095077-G-A

168944459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69095332-T-A

168944459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69095332-T-C

168944644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69095768-C-T

168944804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69095930-T-C

168944872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69095997-G-A

168944872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69095997-G-T

168944887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69096012-G-A

168944887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69096012-G-T

http://identifiers.org/hco/2/GRCh38#168945112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69096226-C-A

168945222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69096364-G-C

168945247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69096389-T-C

168945716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69096781-C-T

168945844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69096927-T-C

168946221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69097560-C-T

168946303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69097643-G-A

168946303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69097643-G-C

168946380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69097719-A-G

168946676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69098448-A-G

168946682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69098454-G-T

168946808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69098568-G-T

168946841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69098593-C-T

http://identifiers.org/hco/2/GRCh38#168947440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69099492-C-A

168947720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69099763-G-A

http://identifiers.org/hco/2/GRCh38#168947760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69099801-C-A

168947799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69099840-G-A

168947998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69100140-G-T

168948043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69100190-G-A

168948050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69100196-T-A

168948179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69100302-G-A

168948179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69100302-G-T

168948217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69100341-G-A

http://identifiers.org/hco/2/GRCh38#168948270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69101095-C-A

168948398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69101223-A-T

168948612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69101432-A-G

168948949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69102931-T-A

168948949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69102931-T-C

168957559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69103897-C-T

168957571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69103909-A-T

168957797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104103-C-T

168957843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104149-T-C

168957843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104149-T-G

168957899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104241-G-A

168957899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104241-G-T

http://identifiers.org/hco/2/GRCh38#168957905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69104283-A-C

168957905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104283-A-T

168957914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104292-A-G

168957955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104333-T-C

168957987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69104365-A-G

http://identifiers.org/hco/2/GRCh38#168958033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69104411-C-A

168958033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69104411-C-T

168958081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69104459-C-T

168958187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104547-G-T

http://identifiers.org/hco/2/GRCh38#168958203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69104563-C-A

168958203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104563-C-T

168958234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104595-G-A

168958234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69104595-G-T

168960624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69105350-T-C

168960634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69105362-C-T

168961199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69105605-G-A

168961528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69105925-T-C

168961864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69106465-G-A

168961864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69106465-G-T

http://identifiers.org/hco/2/GRCh38#168962280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69106864-C-A

168962294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69106878-G-A

168962845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69106983-G-C

http://identifiers.org/hco/2/GRCh38#168962850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69106988-C-A

168962951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69107079-T-G

168962968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69107092-T-A

168963039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69107152-C-G

168963039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69107152-C-T

168963407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69107516-T-C

168963528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69107612-T-C

168963866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69107755-C-G

168964088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108000-G-A

168964088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108000-G-T

168964100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108012-T-A

168964100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108012-T-C

168964100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108012-T-G

168964113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108024-C-G

168964113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108024-C-T

168964116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108027-A-G

168964116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108027-A-T

168964155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108058-T-G

http://identifiers.org/hco/2/GRCh38#168964186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69108095-A-C

168964186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108095-A-T

http://identifiers.org/hco/2/GRCh38#168964296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69108202-C-A

168964296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69108202-C-T

168964378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108287-A-G

http://identifiers.org/hco/2/GRCh38#168964445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69108352-C-A

168964478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108385-G-A

168964478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108385-G-C

168964792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108513-T-C

168964987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108684-T-G

168965685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108816-A-G

168965883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108988-G-A

168965894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69108999-C-T

168966050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69109150-A-G

168966201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69109314-T-A

168966363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69109487-T-C

168966548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69109713-A-G

http://identifiers.org/hco/2/GRCh38#168966732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69109907-C-A

168966888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69110064-A-T

168967059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69110223-C-T

168967643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69110826-T-C

168967887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112116-C-T

168968301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112800-G-A

168968301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112800-G-C

168968301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112800-G-T

168968310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112822-T-C

168968357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112869-G-A

168968357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112869-G-T

168968361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69112873-T-G

168968801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114383-T-A

168968801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114383-T-C

168968848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114422-T-G

168968864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114438-A-G

168968872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114446-C-T

http://identifiers.org/hco/2/GRCh38#168969101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69114662-C-A

168969101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114662-C-T

168969130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114672-A-G

168969211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114752-G-A

168969211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114752-G-C

168969211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114752-G-T

168969227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114804-T-C

168969275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69114859-T-C

168969375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69114959-T-C

168969402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69114986-T-C

168969411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 69114995-G-A

168969469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69115053-T-C

168969470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69115054-G-A

168969470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69115054-G-T

168969490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69115074-T-A

168969490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69115074-T-C

http://identifiers.org/hco/2/GRCh38#168969604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69115188-C-A

168969604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115188-C-T

168969638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115222-G-A

168969638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115222-G-T

http://identifiers.org/hco/2/GRCh38#168969675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69115257-C-A

168969675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115257-C-T

168969760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115340-C-T

http://identifiers.org/hco/2/GRCh38#168969797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69115362-C-A

168969876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115440-G-A

168969907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115470-T-A

168969907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115470-T-C

168969907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115470-T-G

168969979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115527-G-A

168969979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69115527-G-T

168970147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69115656-G-A

168970147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69115656-G-T

168970186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69115695-T-C

168970484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69115950-T-A

168970484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69115950-T-C

168970509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69115973-G-A

168970509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69115973-G-T

http://identifiers.org/hco/2/GRCh38#168970540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69116004-C-A

http://identifiers.org/hco/2/GRCh38#168970568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69116032-C-A

168970568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69116032-C-T

168970635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116097-G-C

168970635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116097-G-T

168970657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116117-C-T

http://identifiers.org/hco/2/GRCh38#168970678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69116140-C-A

168970678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116140-C-G

168970719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116181-T-A

168970719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116181-T-C

168970737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116199-T-A

168970737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116199-T-C

168970966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116466-G-A

168971003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116503-A-G

http://identifiers.org/hco/2/GRCh38#168971671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69116856-C-A

168971818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69116983-T-G

168971841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69117003-G-A

168971841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69117003-G-C

168971841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69117003-G-T

168971862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 69117024-G-C

168971916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 69117078-T-C

168972058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69117220-G-A

168972080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117239-T-G

http://identifiers.org/hco/2/GRCh38#168972126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69117285-A-C

168972149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117308-G-T

168972170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117329-A-G

168972254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117411-G-A

168972412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117564-T-C

168972427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117579-A-G

168972436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117588-A-T

168972531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117682-G-A

168972531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117682-G-T

http://identifiers.org/hco/2/GRCh38#168973663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69117891-C-A

168973663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69117891-C-T

168973733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: stop gained
orthologous variants: 69117961-A-T

168973751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69117979-T-C

168973751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: missense variant
orthologous variants: 69117979-T-G

168973793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69118021-A-T

168973883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69118115-T-G

168973984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69118243-T-C

168974092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69118333-C-T

168974387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69118818-A-G

168975872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119039-G-T

168975887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119054-C-T

168975943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119115-T-C

168976033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69119210-A-G

168976033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69119210-A-T

168976172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119332-C-T

168976183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119343-A-T

168976319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119467-G-A

168976362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119506-C-G

168976362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119506-C-T

168976508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69119648-T-C

168976631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69119764-A-G

168976681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 69119814-T-C

http://identifiers.org/hco/2/GRCh38#168976777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69120008-C-A

168976777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120008-C-T

168977009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120278-A-G

168977046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120333-T-A

168977046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120333-T-C

168977046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120333-T-G

168977076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120378-T-C

168977353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120604-G-A

168977499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120740-C-G

168977508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120749-C-T

168977520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69120761-A-G

168978963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69121542-G-A

http://identifiers.org/hco/2/GRCh38#168978977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69121556-C-A

168979021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69121596-G-A

http://identifiers.org/hco/2/GRCh38#168979862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69122281-A-C

168979862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122281-A-G

168979862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122281-A-T

http://identifiers.org/hco/2/GRCh38#168980005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69122452-C-A

168980054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122500-C-T

168980068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122505-A-G

168980069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122506-G-T

168980113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122553-T-A

168980113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122553-T-G

168980180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122611-A-G

http://identifiers.org/hco/2/GRCh38#168981767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69122803-C-A

168981820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122855-C-G

168981851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69122886-G-T

168982418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69123464-A-G

168982422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69123468-T-C

168982660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69123693-G-A

168982660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69123693-G-C

168983326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69125586-T-C

168983357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69125618-A-G

168983485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69125741-T-C

168983485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69125741-T-G

168983527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69125782-T-C

168983579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69125836-T-C

168983862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126084-C-T

168984417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126176-T-C

168984492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126263-T-G

168984683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126402-T-G

168984751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126469-G-T

168986164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69126710-G-A

168986164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: stop gained
orthologous variants: 69126710-G-C

168986164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: stop gained
orthologous variants: 69126710-G-T

http://identifiers.org/hco/2/GRCh38#168986317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69126863-C-A

168986317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126863-C-T

168986338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126884-T-C

168986339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126885-G-A

168986339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69126885-G-T

168986537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69127132-A-G

168986551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69127146-G-A

168986591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69127187-T-A

168986602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69127198-G-A

168988455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69128972-T-G

168988540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129012-A-G

168988579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129051-G-C

168988655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129128-G-A

168988655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129128-G-T

168988756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129224-C-T

168988758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129226-A-G

168988779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129241-A-G

168988841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129299-G-A

168988942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129382-A-T

168989125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129571-T-C

168990445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129636-G-T

168990476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129698-T-C

168990520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129742-T-C

http://identifiers.org/hco/2/GRCh38#168990547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69129768-A-C

168990559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129779-T-A

168990604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129812-A-G

168990604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129812-A-T

168990616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129824-G-T

http://identifiers.org/hco/2/GRCh38#168990654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69129941-A-C

168990654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69129941-A-G

168990715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130041-G-A

168990715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130041-G-T

http://identifiers.org/hco/2/GRCh38#168990720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69130046-C-A

168990720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130046-C-T

168990758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130101-G-A

168990758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130101-G-C

168990758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130101-G-T

168990908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69130254-C-G

168990908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69130254-C-T

168991058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130383-G-A

168991058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130383-G-T

168991424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130739-G-A

168991468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130778-C-T

168991497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69130809-T-C

168991629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69131941-T-C

168992037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69132466-G-A

168992047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69132476-C-T

168992097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69132575-T-C

http://identifiers.org/hco/2/GRCh38#168992191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69132700-A-C

168992531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133068-T-C

168992541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133078-A-G

168992645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133184-T-A

168992645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133184-T-G

168992700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133239-C-T

168992703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133242-G-A

168992723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133263-G-A

http://identifiers.org/hco/2/GRCh38#168992730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69133270-C-A

168992760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133345-C-T

168992883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133476-T-C

168992960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133547-G-A

168992982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133602-T-A

168992982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133602-T-G

168993113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133726-G-A

168993344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69133907-C-T

168993581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134130-A-G

168993581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134130-A-T

168993642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134187-G-A

168993642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134187-G-C

168993642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134187-G-T

168993683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134228-A-G

168993747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69134317-G-A

168993819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69134389-G-A

168993819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69134389-G-C

168993867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 69134437-G-A

http://identifiers.org/hco/2/GRCh38#168993987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69134537-C-A

168994129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134668-G-A

168994251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134754-T-A

168994351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134838-G-A

168994353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134840-G-T

http://identifiers.org/hco/2/GRCh38#168994367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69134900-C-A

168994367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69134900-C-T

168994569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69135086-A-G

168994644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69135166-C-T

168994703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69135228-A-G

168994823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69135336-G-A

168995313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69136813-A-G

168995317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69136817-C-G

168995317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69136817-C-T

168995332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69136832-T-C

168995366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 69136866-C-T

168995378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 69136878-T-A

168995378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 69136878-T-C

168995382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 69136882-T-C

168995431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 69136931-A-G

168995558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137073-C-T

http://identifiers.org/hco/2/GRCh38#168995564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69137079-A-C

168995564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137079-A-G

168995586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137112-G-A

168995586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137112-G-T

168995630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137155-G-T

168995636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137161-T-C

168995680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137201-T-C

168995824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137344-T-C

168995843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69137363-G-A

http://identifiers.org/hco/2/GRCh38#168995861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69137380-A-C

http://identifiers.org/hco/2/GRCh38#168995976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69138163-A-C

168995976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138163-A-G

168995976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138163-A-T

http://identifiers.org/hco/2/GRCh38#168996023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69138195-C-A

168996113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138287-A-G

168996191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138347-A-G

168996251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138407-T-C

http://identifiers.org/hco/2/GRCh38#168996329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69138500-C-A

168996559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138727-G-T

168996582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138750-A-G

168996589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138757-T-C

168996620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138788-G-A

168996620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138788-G-T

168996668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69138836-A-G

168996704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69138872-G-A

168996704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: missense variant
orthologous variants: 69138872-G-T

168996781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69138947-A-G

168997166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69139051-C-T

168997275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69139151-T-G

168997326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69139204-T-A

168997326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69139204-T-C

168997427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69139284-G-C

169010436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69151727-C-T

http://identifiers.org/hco/2/GRCh38#169010576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69151853-A-C

169010644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69151918-T-C

169010966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69152261-T-C

169011430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69152596-T-C

169011527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69152688-T-A

http://identifiers.org/hco/2/GRCh38#169011608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69152756-A-C

169011608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69152756-A-G

http://identifiers.org/hco/2/GRCh38#169011754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69152897-C-A

169011790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69152938-T-C

169011855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69153010-G-C

169012006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69153255-T-G

http://identifiers.org/hco/2/GRCh38#169012069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69153311-C-A

169012095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153338-G-A

169012095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153338-G-C

169012191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153426-C-G

169012287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153523-G-A

169012317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153552-T-C

169012376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153610-G-C

http://identifiers.org/hco/2/GRCh38#169012718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69153800-C-A

169012749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69153820-A-G

169012755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153826-G-A

169012762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, undefined
orthologous variants: 69153833-G-A

169012913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69153855-G-T

169013018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69153953-A-G

http://identifiers.org/hco/2/GRCh38#169013153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69154076-C-A

169013153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154076-C-G

169013153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154076-C-T

http://identifiers.org/hco/2/GRCh38#169013190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69154113-A-C

169013190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154113-A-G

169013286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69154190-A-G

169013286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: missense variant
orthologous variants: 69154190-A-T

169013480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: synonymous variant
orthologous variants: 69154384-G-A

169013525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154429-G-A

169013525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154429-G-C

169013525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154429-G-T

169013551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154455-A-G

169013601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154522-T-A

http://identifiers.org/hco/2/GRCh38#169013608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69154529-C-A

169013608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154529-C-T

169013626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154548-G-A

169013626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154548-G-T

http://identifiers.org/hco/2/GRCh38#169013633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69154555-C-A

169013660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154577-T-C

169013719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154629-T-C

169013781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154674-C-T

169013921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69154790-C-T

169014042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155253-C-T

169014051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155262-A-G

169014166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155350-A-G

169014188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155372-A-G

169014195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155379-A-T

169014251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155434-A-G

169014274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155454-A-G

169014276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155456-T-C

169014276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69155456-T-G

169016175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69157576-T-G

169016299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69157693-T-A

169016326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69157712-A-G

169016343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69157729-G-A

169016494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69157919-G-T

http://identifiers.org/hco/2/GRCh38#169016666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69158215-A-C

169016685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158234-G-A

169016685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158234-G-C

169016685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158234-G-T

169016721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158265-T-A

169016721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158265-T-C

169016730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158274-T-A

169016730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158274-T-C

http://identifiers.org/hco/2/GRCh38#169016767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69158310-C-A

169016844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158384-G-A

169016844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158384-G-C

169016844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158384-G-T

169017027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158659-G-A

169017027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158659-G-C

169017073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158705-G-A

169017290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69158932-C-T

169017439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159110-A-G

169017439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159110-A-T

169017721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159297-G-A

169017805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159373-G-A

169017805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159373-G-C

169017805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159373-G-T

http://identifiers.org/hco/2/GRCh38#169017841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69159410-C-A

169017841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159410-C-T

169017898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159464-G-A

169017898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159464-G-T

169017909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159474-T-C

http://identifiers.org/hco/2/GRCh38#169017927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69159497-C-A

169017927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159497-C-T

169017931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159501-A-G

169017941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69159511-T-C

169017981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, missense_variant
orthologous variants: 69159551-A-G

169017986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, missense_variant
orthologous variants: 69159557-C-T

169018056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: missense variant
orthologous variants: 69159620-T-C

169018150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 69159714-A-G

169018159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69159723-A-G

169018225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159781-A-G

169018290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69159862-T-A

169018894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69161032-C-G

169018944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69161064-G-A

169019025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69161125-G-A

169019079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69161177-T-G

169019125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69161225-C-T

169021987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69164980-C-T

169025196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69168764-T-A

169025196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69168764-T-C

169025196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69168764-T-G

169025432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169076-G-A

169025467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169108-T-C

169025476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169117-A-G

169025776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169402-C-T

169025939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169547-G-T

169026050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169620-G-C

169026050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169620-G-T

169026181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169706-A-G

169026213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169735-T-A

169026261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169763-T-C

169026333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169814-C-T

169026355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169834-A-G

169026356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69169835-G-A

169027373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171172-T-C

169027395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171198-A-G

169027459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171257-C-T

169027467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171265-C-T

169027478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171276-G-A

169027519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171315-T-G

169027615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171401-G-T

169027621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171407-A-G

http://identifiers.org/hco/2/GRCh38#169027672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69171455-A-C

169027712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171491-C-G

169027856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171628-T-C

http://identifiers.org/hco/2/GRCh38#169027963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69171796-C-A

169027963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171796-C-T

169027973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171814-C-T

169027975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171816-A-G

169027976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171817-T-C

169028025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171866-T-G

169028031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171872-T-C

169028125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69171968-C-T

http://identifiers.org/hco/2/GRCh38#169028248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69172084-C-A

169028345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172148-G-T

169028370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172172-G-A

169028540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172311-T-G

169028570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172345-G-T

169028661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172429-G-T

169031076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172696-G-A

169031076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172696-G-T

169031175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172793-G-A

169031200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172836-G-A

169031200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: intron variant
orthologous variants: 69172836-G-T

http://identifiers.org/hco/2/GRCh38#169031265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69172901-C-A

169031265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42
most severe consequence: 5 prime UTR variant
orthologous variants: 69172901-C-T