118839287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49829969-G-A

118839287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49829969-G-T

118839315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49829993-T-C

118839844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49830193-A-G

118839871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49830234-T-C

118839973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49830349-C-T

118840030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49830397-T-G

118840119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49830485-T-C

118840119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49830485-T-G

118840257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3 prime UTR variant
orthologous variants: 49830633-A-G

118840325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830693-C-T

118840381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830746-A-G

118840415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830775-T-G

118840430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830790-T-C

118840463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830836-T-C

118840530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830884-A-G

118840626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830969-C-T

118840660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830997-A-G

118840660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49830997-A-T

118840678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831023-T-C

118840678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831023-T-G

118840680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831025-T-C

118840680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831025-T-G

http://identifiers.org/hco/5/GRCh38#118840689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49831034-C-A

118840689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831034-C-T

118840690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831035-A-T

118840698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831043-A-T

http://identifiers.org/hco/5/GRCh38#118840729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49831085-C-A

118840729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831085-C-T

118840732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831088-T-C

118840732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831088-T-G

118840735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831112-G-T

118840805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831271-T-C

118840805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831271-T-G

118840814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831280-C-T

118840847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49831329-A-T

118840964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49831444-G-A

118840964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49831444-G-C

118840977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49831457-C-T

118840998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 49831478-A-G

118841235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49831709-T-C

118841235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49831709-T-G

118841337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49831771-A-G

118841337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49831771-A-T

118845932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49831996-A-G

118847113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49832353-T-C

118847319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49832548-G-C

118847539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49832831-G-A

http://identifiers.org/hco/5/GRCh38#118847608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49832903-C-A

118847620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49832912-C-T

118847632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49832924-C-T

118847671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49832963-A-G

118847896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49833169-A-G

118847987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49833231-T-C

118848038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49833285-A-G

118848138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 49833374-A-G

118848201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 49833437-G-A

118848201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49833437-G-C

118848201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49833437-G-T

118848486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49833726-C-T

118864844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49838388-T-C

118865128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49839294-C-T

118865947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49839616-A-G

118865988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49839682-G-T

118866020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49839714-C-G

118891019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49839837-G-A

118891046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49839864-C-T

118891071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49839889-T-C

118891250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49840055-T-C

118891365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49840165-A-G

118891375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49840175-C-T

118896109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49843598-C-G

118896287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49843764-A-G

118896375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49843850-T-C

118896412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49843884-T-A

118896455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49843928-T-A

http://identifiers.org/hco/5/GRCh38#118896486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49843954-C-A

http://identifiers.org/hco/5/GRCh38#118896496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49843964-C-A

118896496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49843964-C-T

118896595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49844055-A-G

118927415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49855490-T-C

118927477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49855543-C-T

118927660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49855734-T-C

118927766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49855828-G-C

http://identifiers.org/hco/5/GRCh38#118927933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49855988-A-C

http://identifiers.org/hco/5/GRCh38#118928393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49856543-C-A

118928548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856700-G-A

118928548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856700-G-T

118928561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 49856713-G-A

118928582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 49856734-A-G

118928582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 49856734-A-T

http://identifiers.org/hco/5/GRCh38#118928599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49856751-C-A

118928599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856751-C-T

118928604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856756-A-G

118928642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856794-T-C

http://identifiers.org/hco/5/GRCh38#118928671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49856823-C-A

118928671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856823-C-G

118928671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856823-C-T

118928704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856856-G-A

118928704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 49856856-G-T

118928719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856871-G-A

118928719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49856871-G-C

118928786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49856937-T-C

http://identifiers.org/hco/5/GRCh38#118928865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49856997-A-C

118928866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49856998-G-C

118928866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49856998-G-T

118939155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857134-G-A

118939266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49857250-G-T

118939283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 49857267-T-C

118939319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857299-G-C

118939319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857299-G-T

118939325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857305-T-A

118939427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857479-A-G

http://identifiers.org/hco/5/GRCh38#118939479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49857519-A-C

118939799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857840-C-T

118939854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857891-A-G

http://identifiers.org/hco/5/GRCh38#118939918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49857945-A-C

118939918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49857945-A-G

http://identifiers.org/hco/5/GRCh38#118939971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49857970-A-C

118940373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49858174-A-T

118940570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49859004-A-G

118940676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49859136-T-C

118940685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49859145-C-G

118940820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49859291-T-G

118942664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49859823-C-T

118943170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49860042-G-A

118943170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49860042-G-C

118944034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49860958-G-A

118944331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861246-A-G

118944353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861262-G-C

118944489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861378-A-T

http://identifiers.org/hco/5/GRCh38#118944495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49861384-A-C

118944495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861384-A-G

118944499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861388-T-C

118944586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 49861463-G-A

118944586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49861463-G-C

118944606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49861483-G-C

118944607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 49861484-G-A

118944607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49861484-G-T

118944609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49861486-G-A

118944628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 49861505-C-T

118944670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861540-T-A

118944670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861540-T-C

http://identifiers.org/hco/5/GRCh38#118944674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49861544-A-C

118944697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861565-T-C

118944697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861565-T-G

118944715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861584-A-T

118944718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861587-G-T

http://identifiers.org/hco/5/GRCh38#118944731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49861608-C-A

118944731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861608-C-T

118944744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861622-A-G

118944750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861628-T-G

118945796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49864821-A-G

118945870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49864878-G-A

118945924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49864917-A-T

118946228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49866027-C-T

118946263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49866062-A-T

118946460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49866252-C-T

118952703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49866963-G-T

118953101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49867431-A-G

118953122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49867458-G-C

118953340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868245-C-T

118953420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868321-G-A

118953763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868631-G-A

118953890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868682-C-T

118953904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868697-G-A

118953904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868697-G-C

118953990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868725-G-A

118954046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868784-G-A

http://identifiers.org/hco/5/GRCh38#118954133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49868875-C-A

118954133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49868875-C-T

118954380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49869072-T-G

118955074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49869448-C-T

http://identifiers.org/hco/5/GRCh38#118955116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49869473-A-C

118955116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49869473-A-G

118955367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49870210-T-C

118955421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49870265-G-A

118956259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49870502-G-A

118956259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49870502-G-T

118956479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49870720-G-A

118956677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49870920-G-C

http://identifiers.org/hco/5/GRCh38#118956786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49871051-C-A

118961377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-T

118961609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49874638-C-G

118961619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49874647-T-C

118961632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49874660-A-G

http://identifiers.org/hco/5/GRCh38#118961858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49874894-A-C

118962857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49875523-G-A

http://identifiers.org/hco/5/GRCh38#118966073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49878227-C-A

118966073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49878227-C-T

118966132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49878267-G-A

118966244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49878371-A-G

http://identifiers.org/hco/5/GRCh38#118966255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49878378-C-A

http://identifiers.org/hco/5/GRCh38#118966261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49878384-A-C

118966294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49878420-G-T

118981693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49883674-G-C

118981749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49883730-C-T

118981906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49883958-C-G

118982386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49884834-C-T

118982419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49884868-C-T

118982430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49884882-G-A

http://identifiers.org/hco/5/GRCh38#118982597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49885004-C-A

118982597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49885004-C-T

118987302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49885564-T-C

118987577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49885739-T-A

http://identifiers.org/hco/5/GRCh38#118987670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49885813-C-A

118987746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49885881-C-T

118987773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49885908-G-C

118987845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49885982-T-C

118988301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888395-G-A

118988301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888395-G-C

118988301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888395-G-T

118988304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888398-T-C

118988304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888398-T-G

http://identifiers.org/hco/5/GRCh38#118988318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888412-C-A

118988318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888412-C-G

118988318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888412-C-T

http://identifiers.org/hco/5/GRCh38#118988352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888446-C-A

118988352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888446-C-T

118988353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 49888447-G-A

118988353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888447-G-C

118988353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888447-G-T

118988361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888455-T-A

118988361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888455-T-C

118988363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888457-T-C

118988393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888487-G-A

118988396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888490-G-A

118988396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888490-G-C

118988396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888490-G-T

http://identifiers.org/hco/5/GRCh38#118988398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888492-C-A

118988398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 49888492-C-G

118988398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 49888492-C-T

118988399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888493-G-A

118988405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888499-G-A

118988406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888500-C-T

118988436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888530-G-A

118988436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888530-G-C

118988436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888530-G-T

http://identifiers.org/hco/5/GRCh38#118988437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888531-C-A

118988437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 49888531-C-G

118988437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 49888531-C-T

118988442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888536-G-T

http://identifiers.org/hco/5/GRCh38#118988447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888541-C-A

118988447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888541-C-T

118988451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888545-A-G

118988451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888545-A-T

http://identifiers.org/hco/5/GRCh38#118988465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888559-C-A

118988465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888559-C-T

118988481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, stop_gained, undefined
orthologous variants: 49888575-G-A

118988481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888575-G-C

118988481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888575-G-T

http://identifiers.org/hco/5/GRCh38#118988489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888583-C-A

118988489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888583-C-G

118988489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888583-C-T

http://identifiers.org/hco/5/GRCh38#118988493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888587-C-A

118988493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49888587-C-T

118988497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 49888591-T-C

118988504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 49888598-G-A

118988504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: NMD_transcript_variant, stop_gained, undefined
orthologous variants: 49888598-G-T

http://identifiers.org/hco/5/GRCh38#118988518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#49888612-C-A

118988518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 49888612-C-T

118988538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49888632-A-G

118988538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19334
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49888632-A-T