http://identifiers.org/hco/6/GRCh38#38170803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30436010-C-A

http://identifiers.org/hco/6/GRCh38#38170916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30436090-C-A

38170916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30436090-C-T

38171148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30436264-C-T

38171240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30436345-A-G

http://identifiers.org/hco/6/GRCh38#38171469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30436574-A-C

38171469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30436574-A-G

38171514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30436618-A-G

http://identifiers.org/hco/6/GRCh38#38172459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30437266-C-A

38172459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30437266-C-G

38174113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438569-C-T

38174139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438595-C-T

38174231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438674-T-C

38174325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438776-G-T

http://identifiers.org/hco/6/GRCh38#38174478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30438891-C-A

38174478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438891-C-T

38174484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438897-T-C

38174498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438911-G-A

38174498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438911-G-T

http://identifiers.org/hco/6/GRCh38#38174534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30438944-C-A

38174534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438944-C-G

38174574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438975-G-C

38174574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30438975-G-T

http://identifiers.org/hco/6/GRCh38#38174584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30438985-A-C

http://identifiers.org/hco/6/GRCh38#38174603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30439013-C-A

http://identifiers.org/hco/6/GRCh38#38174645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30439056-C-A

38174655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30439076-A-G

38174753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30439167-A-T

http://identifiers.org/hco/6/GRCh38#38174780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30439193-C-A

38174780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30439193-C-G

38174886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30439287-G-A

38174886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30439287-G-T

38174888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30439289-A-G

38174923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3 prime UTR variant
orthologous variants: 30439292-G-T

http://identifiers.org/hco/6/GRCh38#38174972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30439334-C-A

38174972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 30439334-C-T

38175018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 30439380-G-A

38175260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30439604-C-T

38175334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30439668-A-G

38179412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30440818-G-A

38179428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30440834-G-A

38179428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30440834-G-C

38179820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30441159-A-G

38179825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30441164-G-T

38179830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30441169-G-T

38179840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30441179-C-G

http://identifiers.org/hco/6/GRCh38#38179944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30441306-C-A

38179944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30441306-C-T

http://identifiers.org/hco/6/GRCh38#38180024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30441382-A-C

38180546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30441801-C-G

38180695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30441951-C-T

38180873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30442125-C-T

38181194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30442410-C-T

38182191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30443107-A-G

http://identifiers.org/hco/6/GRCh38#38184580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30444358-A-C

38184728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30444440-C-T

38184791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30444497-T-C

38184940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30444597-G-A

38185444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30445035-C-T

38192404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30447670-G-T

38192667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30447909-G-A

38192667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30447909-G-T

38192704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30447923-G-A

38192704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30447923-G-T

38192716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30447935-A-G

38193892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30449175-T-C

38193892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30449175-T-G

38194549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30449640-T-C

38194611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30449715-G-T

38195161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30450145-G-A

http://identifiers.org/hco/6/GRCh38#38195174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30450158-C-A

38208556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30454438-G-A

38208750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30454599-C-T

38208973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30454760-G-A

38209158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30454911-G-A

38209647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30455334-C-G

38209674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30455375-G-C

38210136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30455790-C-T

38210273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30455928-C-T

38210424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30456070-T-A

38210447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30456092-G-A

38210447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30456092-G-T

http://identifiers.org/hco/6/GRCh38#38210454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30456099-A-C

38210600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30456208-G-C

38211059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30456610-A-G

38211110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30456650-G-A

38211769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30457186-C-G

38211967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30457781-T-C

38212117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30457909-G-T

38212206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30457969-T-C

38212368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458106-G-A

38212416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458141-G-A

38212571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458343-G-A

38212805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458551-C-G

38212805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458551-C-T

38212848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458583-C-G

38212918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458647-C-T

38213025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30458748-T-C

http://identifiers.org/hco/6/GRCh38#38213063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30458787-A-C

http://identifiers.org/hco/6/GRCh38#38213374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30459100-C-A

38213377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30459103-T-C

38213428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30459153-C-T

38214108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30459557-C-T

38214432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30459842-G-C

38214585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30459930-A-T

38214619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30459959-G-A

38214719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460088-A-G

38214722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460091-C-T

38214839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460206-T-C

38214997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460360-A-G

38215125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460487-G-A

38215148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460512-T-G

38215194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460558-T-C

38215194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460558-T-G

38215265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30460629-T-C

38217656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30461838-G-T

38217763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30461862-C-T

38217933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30462007-A-G

38218074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30462150-G-A

http://identifiers.org/hco/6/GRCh38#38218406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30462608-C-A

38218439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30462662-C-G

38218487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30462707-G-C

http://identifiers.org/hco/6/GRCh38#38218554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30462770-A-C

38218554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30462770-A-G

38218780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30462947-C-T

http://identifiers.org/hco/6/GRCh38#38219955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30463680-A-C

38220182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30463881-A-G

http://identifiers.org/hco/6/GRCh38#38220509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30464099-C-A

38220808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30464392-C-T

38220839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30464423-C-T

38221174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30464741-G-A

38221587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30465077-C-T

38221679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30465163-T-C

38221700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30465187-T-A

38221700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30465187-T-C

38223709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30465922-G-A

http://identifiers.org/hco/6/GRCh38#38224444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30466337-C-A

38224770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30466665-A-T

38224842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30466728-G-A

38225261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467062-A-G

38225285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467086-G-A

38225421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467186-C-T

38225495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467256-C-G

38225646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467402-T-C

38225859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467556-T-A

38226060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467717-T-C

38226277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30467865-C-T

38226596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30468091-T-G

38226737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30468996-G-C

http://identifiers.org/hco/6/GRCh38#38226752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30469011-A-C

38226756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30469015-T-C

38226772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30469031-C-T

38226801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30469073-G-A

38227006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30469278-C-T

38229356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30470321-A-G

38229409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30470369-A-G

38229579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30470528-T-C

38229854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30470774-T-C

38230975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30472440-G-A

38231233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30472658-G-A

38231642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30473015-G-A

http://identifiers.org/hco/6/GRCh38#38231849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30473182-C-A

38231915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30473242-T-C

38233331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30475468-A-G

38234159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30476554-G-A

38234644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30476961-G-A

38234644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30476961-G-C

http://identifiers.org/hco/6/GRCh38#38234647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30476964-C-A

38235005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30477222-T-C

http://identifiers.org/hco/6/GRCh38#38235613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30477771-A-C

38235770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30477890-T-C

38236982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30478355-G-A

38237275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30479302-T-G

http://identifiers.org/hco/6/GRCh38#38237348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30479371-C-A

http://identifiers.org/hco/6/GRCh38#38237572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30479770-C-A

38237612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30479795-C-T

38239583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30480270-C-T

38239763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30480441-T-C

38239835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30480509-C-G

http://identifiers.org/hco/6/GRCh38#38239892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30480569-A-C

38239939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30480614-C-T

38240162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30480827-C-T

38240253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30480898-G-C

38240253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30480898-G-T

38240525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30481153-T-C

38240911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30481513-T-G

38242200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30482686-T-C

38242200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30482686-T-G

38242262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30482746-T-C

http://identifiers.org/hco/6/GRCh38#38242630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30483227-C-A

38242630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483227-C-T

38242706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483279-C-T

38242743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483299-G-C

38242754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483310-G-C

38242754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483310-G-T

38242799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483315-C-G

38242799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483315-C-T

38243390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30483762-A-G

38244264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30484465-A-T

38244298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30484499-C-T

38244531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30484720-C-G

38244531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30484720-C-T

38245940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30485039-T-G

38246188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30485236-A-G

38246518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30485464-G-A

38247067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486250-T-A

http://identifiers.org/hco/6/GRCh38#38247250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30486415-A-C

38247250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486415-A-G

38247250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486415-A-T

38247319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486486-C-T

38247348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486518-G-T

38247482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486650-G-A

38247687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486745-C-T

38247960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486970-T-C

38247980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30486996-T-C

38249806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30488415-A-G

http://identifiers.org/hco/6/GRCh38#38249817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30488426-C-A

38250240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30488796-A-G

38250240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30488796-A-T

38252280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30490070-G-A

http://identifiers.org/hco/6/GRCh38#38252447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30490178-A-C

38252447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30490178-A-G

38252590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30490323-G-A

38252592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30490325-A-G

38252674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30490404-T-C

38253755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30490842-A-T

38253771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30490858-G-C

38254233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30491746-T-A

38254895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30492466-C-T

38255188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30492754-T-C

38255326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30492857-T-C

38255353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30492881-T-C

38256115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30493595-G-T

38256288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30493751-G-A

38256368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30493802-T-G

38256477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 30493896-G-A

38256539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30493957-G-T

38256546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30493964-G-T

http://identifiers.org/hco/6/GRCh38#38256648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30494052-C-A

38256728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30494131-A-G

http://identifiers.org/hco/6/GRCh38#38256745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30494148-C-A

38256745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30494148-C-T

38256798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30494202-T-A

38257355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30494769-G-A

38257476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30494924-T-C

38257477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30494925-G-A

38260345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30496706-A-G

38260402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30496763-G-C

38260538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30496882-A-T

http://identifiers.org/hco/6/GRCh38#38261398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30497378-C-A

38261398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30497378-C-T

38261537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30497522-G-A

38261537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30497522-G-T

38261763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30497745-C-T

38261924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30497891-T-G

38262926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30498882-C-T

38263309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30499251-C-T

38263505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30499443-T-G

38264005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30499757-G-T

38264077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30499780-G-A

38264090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30499793-G-A

38264485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30500100-C-T

38264517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30500127-C-T

38264536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30500138-A-G

38265003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30500543-G-A

38265003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30500543-G-T

38267266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30502343-G-A

38267328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30502397-C-T

38267431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30502515-G-A

38268236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30502839-T-C

38269904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30504343-C-T

38269961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30504403-G-A

38270047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30504487-T-G

38271467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30505894-G-A

38271951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30506312-T-A

38271986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30506350-G-A

38272191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30506563-T-C

38272309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30506654-T-A

38272309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30506654-T-C

38272319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30506664-C-T

38272322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30506667-A-G

38272821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30507141-T-C

38276721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30508515-G-A

38276757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30508549-A-G

38278468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30510104-G-A

38278694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30510329-T-C

38279485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511136-T-C

38279638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511293-G-C

38279654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511316-C-G

38279690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511352-T-C

38279821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511463-G-T

http://identifiers.org/hco/6/GRCh38#38279841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30511483-C-A

38280035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511669-C-T

38280038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511672-G-T

38280093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511716-C-T

http://identifiers.org/hco/6/GRCh38#38280133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30511756-C-A

38280335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30511948-T-C

http://identifiers.org/hco/6/GRCh38#38280419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30512033-C-A

38280419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512033-C-T

38280683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512288-G-A

38280799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512382-C-T

38280980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512540-A-G

38281001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512578-A-G

38281095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512670-C-T

38281128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512704-T-G

38281256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512830-A-G

38281300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512867-T-C

38281322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30512887-T-C

38281448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30513005-T-A

38281987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30513636-C-T

38282068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30513717-T-C

38283019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30514555-T-C

38283956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30515096-T-G

38284110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30515249-T-A

38284165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30515304-C-T

38284612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30515731-T-A

38285197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30516622-A-G

38285225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30516650-T-C

38285430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30516852-G-A

38285537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30516948-G-A

38285988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30517387-C-T

38286159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30517474-T-C

38286175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30517490-C-T

38286229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30517543-A-G

38287822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30518058-A-G

38287822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30518058-A-T

38288148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30518393-A-G

38288500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30518734-G-A

38289742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-A

38305477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30519648-T-A

38305499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30519670-T-C

38305704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30519872-G-A

http://identifiers.org/hco/6/GRCh38#38305728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30519895-C-A

38305728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30519895-C-G

38305728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30519895-C-T

38306205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30520404-G-C

38306379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30520577-T-A

38306785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30522593-G-A

38307422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30523674-T-A

38307466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30523706-C-T

38307733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30523956-T-C

38309702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30524990-C-T

38310128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30525264-G-T

38310134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30525270-C-T

38320498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30525831-C-T

38320545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30525879-A-G

38320969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30526306-C-T

38320970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30526307-G-A

38321003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30526340-G-C

38321290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30526634-T-C

38321668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30527005-C-T

38321785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30527124-T-C

38322041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30527368-C-T

38322106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30527429-G-A

38322108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30527431-C-T

38322377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30527617-A-G

38323086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30528335-C-T

38323344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30528580-A-G

38323421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30528654-G-T

38323540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30528737-T-C

38323659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30528848-C-T

38323663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30528852-T-C

38325399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30529301-A-G

38325400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30529302-A-G

38325955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30529901-T-C

http://identifiers.org/hco/6/GRCh38#38326015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30529958-A-C

38326103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30530270-A-G

38326804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30530919-C-T

38327076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30531240-C-G

38327637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30531811-T-C

38328452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30532747-T-A

http://identifiers.org/hco/6/GRCh38#38328548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30532836-C-A

38328548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30532836-C-T

38328627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30532894-A-G

38330881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30535702-G-A

38330925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30535749-T-C

38332540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538194-T-A

38332540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538194-T-G

38332570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538224-T-A

38332570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538224-T-C

http://identifiers.org/hco/6/GRCh38#38332574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30538228-C-A

38332574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538228-C-T

38336708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538630-G-A

38336756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538671-G-A

38337136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30538978-T-G

http://identifiers.org/hco/6/GRCh38#38338670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30539964-C-A

38339011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30540269-G-A

38340672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549236-T-C

38341293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549894-T-C

38341352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549933-A-G

38341454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30550201-A-G

38341646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30550356-T-C

38341843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30550548-T-C

38342736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551171-C-T

38343063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551494-C-G

38343298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551717-G-A

38343507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551933-C-T

38344130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30552405-G-C

38344156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30552430-A-G

38344200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30552468-G-A

38344204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30552469-A-G

38344823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553039-A-G

38344868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553075-A-G

38344868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553075-A-T

http://identifiers.org/hco/6/GRCh38#38344890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30553099-C-A

38344890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553099-C-G

http://identifiers.org/hco/6/GRCh38#38345145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30553355-C-A

38345145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553355-C-G

38345145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553355-C-T

38345161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553360-G-T

38345168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553367-A-G

38345168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553367-A-T

38345300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553439-T-C

38345314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553450-G-A

http://identifiers.org/hco/6/GRCh38#38345448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30553583-C-A

38345454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553589-G-A

http://identifiers.org/hco/6/GRCh38#38345660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30553804-C-A

38345660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 30553804-C-G

38345660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 30553804-C-T

38345666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 30553810-C-T

38346349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554473-C-T

http://identifiers.org/hco/6/GRCh38#38346541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30554639-A-C

http://identifiers.org/hco/6/GRCh38#38347069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30555103-C-A

38348104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30555545-C-T

http://identifiers.org/hco/6/GRCh38#38348105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30555546-A-C

http://identifiers.org/hco/6/GRCh38#38348205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30555634-A-C

http://identifiers.org/hco/6/GRCh38#38348427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30555873-A-C

http://identifiers.org/hco/6/GRCh38#38348719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30556160-A-C

38349887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30558730-T-C

38350652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30559401-C-T

38352634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30560638-G-A

38352634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30560638-G-T

38352825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30560807-T-C

38353340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30561263-G-A

38353340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30561263-G-C

38353347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30561270-A-G

38354154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30562309-T-G

38354981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30563006-T-C

38354981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30563006-T-G

38355175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30563184-T-C

38355461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30563394-C-G

38355961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30564481-G-A

38355961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30564481-G-C

38355961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30564481-G-T

38356779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565088-T-C

38356866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565180-C-T

38356931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565248-G-C

38356956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565265-T-C

38356959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565268-G-C

38357108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565408-C-T

38357128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565427-G-A

38357214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565478-C-T

38357257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565520-G-A

38357257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565520-G-T

http://identifiers.org/hco/6/GRCh38#38357347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30565551-C-A

38357992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566045-T-A

38358497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566515-G-A

38358497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566515-G-T

38359019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566789-C-T

38359336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566999-C-T

38359685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567369-C-T

38359745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567405-T-C

http://identifiers.org/hco/6/GRCh38#38360526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30568133-C-A

38360570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568177-C-T

38360609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568218-G-T

38360648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568244-T-A

38360857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568418-G-A

http://identifiers.org/hco/6/GRCh38#38361863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30568966-C-A

38362437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30569361-A-G

http://identifiers.org/hco/6/GRCh38#38362479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30569413-A-C

38362581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30569514-G-A

38363492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30570425-T-G

38364095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30571052-G-A

38364177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30571133-A-T

38364349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30571235-T-A

38364349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30571235-T-C

38364848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30573411-G-A

http://identifiers.org/hco/6/GRCh38#38365060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30573569-A-C

38365327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30573794-C-T

38365992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30574685-G-C

38365992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30574685-G-T

38366015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30574706-G-A

38366500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30575147-C-T

38366514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30575182-A-G

38366672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30575351-G-A

38366677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30575356-C-G

38366826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30575497-T-A

38366911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30575582-T-C

38366911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30575582-T-G

38369623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30578245-T-C

http://identifiers.org/hco/6/GRCh38#38370020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30578550-A-C

38370062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30578592-T-C

38370205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30578728-C-T

38370978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30579525-A-G

38371527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30579999-G-A

38371527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30579999-G-C

38371581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30580052-C-G

38371991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30580396-A-G

38372185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30580585-T-A

38372308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30580709-T-C

38372464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30580866-C-T

38372647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30581055-C-T

38372846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30581231-T-C

38372924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30581320-T-C

38372992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30581378-G-C

38373122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30581500-C-T

38373125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30581503-A-G

38373970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582384-T-C

38374303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582752-A-G

38374327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582776-G-A

38374327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582776-G-C

38374327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582776-G-T

38374328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582777-T-C

38374328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582777-T-G

38374329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582778-A-G

38374329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582778-A-T

http://identifiers.org/hco/6/GRCh38#38374370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30582819-C-A

http://identifiers.org/hco/6/GRCh38#38374375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30582824-C-A

38374377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582826-G-A

38374443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582894-T-C

38374553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582957-G-C

38374717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583101-T-C

38374792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583175-C-G

38375084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583399-C-G

38375115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583425-G-T

38375266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583556-C-T

http://identifiers.org/hco/6/GRCh38#38375362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30583615-C-A

38375422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583682-C-T

38375494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583752-C-G

38375662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583920-T-C

38375739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584000-A-G

38376007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584151-T-C

http://identifiers.org/hco/6/GRCh38#38376112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30584219-A-C

38376128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584235-T-C

38376637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584733-T-A

38376713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584809-G-A

38376851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584945-A-T

38376966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30585067-A-G

38376969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30585070-G-T

38377361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30585412-T-C

38377403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30585448-G-C

38383881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30587627-T-G

38384380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30588158-T-C

38384438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30588216-C-G

38384438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30588216-C-T

38384693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30588458-C-T

38384812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30588579-A-G

38384872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30588748-G-C

38384940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30588842-G-A

38385458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589306-A-G

38385462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589310-T-C

38385554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589394-G-A

http://identifiers.org/hco/6/GRCh38#38385641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30589479-A-C

http://identifiers.org/hco/6/GRCh38#38385817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30589659-C-A

38385817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589659-C-T

38385827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589669-C-T

38385831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589673-G-T

38386073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589771-C-T

38386085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30589787-C-T

38386539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30590322-C-T

http://identifiers.org/hco/6/GRCh38#38387286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30590933-C-A

38387300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30590946-G-C

38387827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30591424-G-A

38387920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30591518-T-C

http://identifiers.org/hco/6/GRCh38#38388130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30591724-C-A

38388210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30591803-T-A

38388210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30591803-T-G

38388211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30591804-G-A

38388211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30591804-G-C

http://identifiers.org/hco/6/GRCh38#38388215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30591808-C-A

38388639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30592366-T-G

38388792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30592533-C-T

38389181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30592899-G-A

38389193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30592911-T-C

38389319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30593038-T-A

38389493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30593185-T-G

38389496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30593188-C-T

38390115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30593760-G-A

38390804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30596334-T-C

38391013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30596677-A-G

38391058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30596722-C-T

38391164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30596850-G-A

38391301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30596957-A-G

38391397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30597060-T-C

http://identifiers.org/hco/6/GRCh38#38391450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30597114-C-A

http://identifiers.org/hco/6/GRCh38#38391558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30597222-A-C

38391627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30597292-G-T

38392077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30597731-C-G

38393677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30599126-G-A

38393708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30599147-C-G

http://identifiers.org/hco/6/GRCh38#38397685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30601853-A-C

38397797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30601936-G-C

38397840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30601973-G-T

38397900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30602018-T-C

http://identifiers.org/hco/6/GRCh38#38398175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30602217-C-A

http://identifiers.org/hco/6/GRCh38#38398251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30602290-C-A

38398629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30602625-C-G

http://identifiers.org/hco/6/GRCh38#38399219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30603164-C-A

38399345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30603285-T-C

38399410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30603352-T-C

http://identifiers.org/hco/6/GRCh38#38400555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30604049-C-A

38400555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30604049-C-G

38400634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30604165-T-G

38400880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30604386-A-G

http://identifiers.org/hco/6/GRCh38#38400889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30604395-A-C

38400890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30604396-C-T

38401585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30605245-T-C

38401615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30605275-G-A

38401626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30605285-T-C

38401687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30605345-C-T

38401688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30605346-A-T

38404381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30607364-T-C

http://identifiers.org/hco/6/GRCh38#38404761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30607734-C-A

38405002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30607934-T-A

38405073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30607994-A-G

38405270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30608162-T-A

http://identifiers.org/hco/6/GRCh38#38405367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30608278-A-C

38405509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30608430-T-A

38405547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30608470-A-G

38405671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30608610-G-C

38406111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30609191-T-C

38406250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30609278-T-C

38406517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30609470-G-A

http://identifiers.org/hco/6/GRCh38#38406725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30609665-A-C

38407215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30610324-C-T

38407399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30610501-T-C

38407492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30610569-C-T

38407513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30610588-G-A

38407844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30610895-C-T

38407948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30611001-G-A

38407948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30611001-G-T

38408566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30611421-C-T

38408595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30611450-A-G

38408595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30611450-A-T

38408838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30611705-C-T

38409410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30611979-G-A

38409562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30612126-C-T

http://identifiers.org/hco/6/GRCh38#38409589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30612150-C-A

38409589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30612150-C-G

38409595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30612156-T-C

38409881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30612320-T-C

38413173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

38413316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-G

38413451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

38414007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

http://identifiers.org/hco/6/GRCh38#38414644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-C

38414679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

38414757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-G

38418371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30618560-T-C

38418467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30618672-C-T

38418681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30618930-C-G

38418681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30618930-C-T

38418701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30618957-G-A

38418716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30618971-G-A

38418761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30619014-T-C

http://identifiers.org/hco/6/GRCh38#38419356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30619426-C-A

38419930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30619751-C-T

38420057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30619873-C-T

38420244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30620051-G-A

38420316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30620114-C-T

38421546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30620902-G-A

38421571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30620920-A-T

38421641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30621063-A-G

38421695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30621105-G-A

38421695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30621105-G-T

38421711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30621121-G-T

38422133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30622042-C-T

38422243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30622160-C-T

38422287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30622197-A-G

http://identifiers.org/hco/6/GRCh38#38422317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30622225-C-A

38422587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30622522-A-T

38422710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30622639-G-A

38423786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30622833-A-G

38423966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30623016-G-A

38424357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30623924-T-C

38426062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30624522-C-G

http://identifiers.org/hco/6/GRCh38#38427508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30624849-C-A

38427508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30624849-C-T

38427563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30624948-G-A

38427567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30624952-G-C

38427629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30625036-T-C

38428020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30625371-G-C

38436335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30628995-G-A

38436438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30629047-C-T

38437487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30629571-G-A

38437487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30629571-G-T

38437552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30629634-C-T

38437746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30629811-G-A

38438048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30630062-G-C

38438057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30630071-G-A

38438059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30630074-G-A

38439876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30630970-G-T

38439912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30631000-G-C

38440239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30631289-C-G

38440544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30631578-C-G

38440859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30631853-G-A

38440945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30631910-C-T

38441016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30631962-G-C

38441048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30631994-A-G

38441172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30632061-G-A

38441253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30632112-T-G

38441303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30632161-T-G

38441421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30632282-A-G

38442127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30633525-G-A

38443038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30633828-C-G

38443207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30633986-G-A

38443477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30634252-G-A

38445131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30634606-G-C

38445438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30634886-C-T

38445573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30635013-G-T

38445719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30635142-T-C

38445971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30635351-C-T

38445974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30635354-T-C

38446123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30635538-C-G

38448930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30636760-T-C

38449016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30636845-T-C

38449100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30636930-T-A

http://identifiers.org/hco/6/GRCh38#38449287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30637089-A-C

38451829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30637865-C-T

38452191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30638138-T-C

38452229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30638175-G-A

38452245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30638189-G-T

38452648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30638560-G-C

38453263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30639151-A-G

38453416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30639306-C-T

38453807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30639656-G-A

38454070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30639884-T-C

http://identifiers.org/hco/6/GRCh38#38454173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30639969-C-A

38454173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30639969-C-G

38454829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30640215-G-A

38456522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30641231-A-G

38456904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30641885-A-T

38456924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30641905-G-A

38457177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30642164-C-G

38457177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30642164-C-T

http://identifiers.org/hco/6/GRCh38#38457184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30642171-C-A

38457434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30642327-G-A

38457701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30642561-T-G

38458473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30642766-G-A

38458758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643041-A-G

38459623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643489-C-T

38459643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643513-G-T

38459660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643530-T-C

38459660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643530-T-G

38459921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643809-C-T

38459968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643842-T-C

38460002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643870-G-C

38460072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30643914-A-G

http://identifiers.org/hco/6/GRCh38#38460150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30643989-A-C

38460166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30644005-G-T

38460471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30644295-A-G

38460477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30644301-G-A

38460492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30644316-T-C

38460554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30644372-A-T

38467819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30647486-A-G

38468365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30647861-C-T

38468591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30648095-T-C

38468742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30648230-T-C

38469636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30648677-T-C

38469849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30648882-T-C

38470243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649220-G-A

38470272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649246-C-G

38470484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649426-C-T

38470499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649442-G-A

38470533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649476-G-A

38470891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649757-C-T

38470933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649793-G-A

38470936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649796-C-G

38470936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649796-C-T

38470955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649814-A-G

38470956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649815-G-A

38470956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30649815-G-C

38471229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30650219-C-T

http://identifiers.org/hco/6/GRCh38#38471383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30650332-A-C

38471390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30650339-C-T

http://identifiers.org/hco/6/GRCh38#38471393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30650342-C-A

38471527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30650445-T-C

http://identifiers.org/hco/6/GRCh38#38471713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30650478-C-A

38471713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30650478-C-G

38472014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30650750-G-C

38472056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30650788-T-C

38472544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651272-T-C

38472572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651301-T-C

38472628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651342-A-G

38472754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651464-T-C

38472754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651464-T-G

38472755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651465-C-T

http://identifiers.org/hco/6/GRCh38#38472823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30651529-C-A

38472823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651529-C-T

38473214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30651812-G-C

http://identifiers.org/hco/6/GRCh38#38473520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30652096-C-A

http://identifiers.org/hco/6/GRCh38#38474733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30652806-A-C

38474838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30652921-G-C

38475087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30653291-A-G

38475413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30653723-G-A

38475550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30653904-C-G

38476012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30654303-T-A

38476202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30654484-C-T

38476368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30654643-G-C

38476401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30654677-G-C

38476460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30654736-T-C

38477036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30655301-T-C

38477309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30656066-T-G

http://identifiers.org/hco/6/GRCh38#38477430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30656164-A-C

38477455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30656184-C-G

http://identifiers.org/hco/6/GRCh38#38477594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30656317-C-A

38477621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30656343-T-C

38477847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30656529-C-T

38478598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30660197-T-C

38478783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30660380-G-A

38479131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30660707-G-A

http://identifiers.org/hco/6/GRCh38#38479260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30660833-C-A

38479260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30660833-C-T

38479315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30660887-C-G

38479335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30660914-C-T

38480053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30661234-G-A

38480070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30661251-G-A

38480664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30661815-C-T

38480691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30661841-C-T

http://identifiers.org/hco/6/GRCh38#38481002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30662084-C-A

38481025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30662105-C-T

38481166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30662233-A-G

38481182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30662249-T-C

38481195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30662262-T-A

http://identifiers.org/hco/6/GRCh38#38481523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30662569-C-A

38481543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30662588-G-A

38481543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30662588-G-T

38481584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30662630-G-T

http://identifiers.org/hco/6/GRCh38#38481638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30662671-C-A

38481788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant, undefined
orthologous variants: 30662807-T-C

38482093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30663064-G-C

38482093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30663064-G-T

38482679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30663923-G-A

38482907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30664148-C-G

38483151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30664354-C-T

http://identifiers.org/hco/6/GRCh38#38483532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30664718-C-A

38483532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30664718-C-T

38483817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30664980-G-C

38483900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30665050-T-C

38487110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30665416-A-G

38487599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30665944-G-A

38487599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30665944-G-C

38487643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30665988-A-G

38487660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30666007-G-A

38487684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30666031-G-A

38488547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30666385-C-T

38488674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30666551-G-T

38488881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30666777-T-A

38489588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30667437-T-C

38489768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30667610-C-T

38489790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30668303-T-C

http://identifiers.org/hco/6/GRCh38#38490034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30668560-C-A

http://identifiers.org/hco/6/GRCh38#38490036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30668562-A-C

38490225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30668717-A-G

38490747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30668881-G-A

38490810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30668937-T-C

38490937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30670996-A-G

38491185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671404-T-C

38491196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671415-G-A

38491307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671529-G-T

38491416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671631-T-C

38491425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671640-T-A

38491435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671650-G-C

38491459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671673-A-G

38491752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30671940-A-G

38491916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30672125-T-C

38492225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30672390-C-T

38492284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30672443-C-G

38492598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30672638-T-C

38492793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30672845-C-T

http://identifiers.org/hco/6/GRCh38#38492984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30673030-C-A

38493264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30673236-T-C

http://identifiers.org/hco/6/GRCh38#38493347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30673322-C-A

38493347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30673322-C-T

38493574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30673495-G-C

38493748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30673646-G-A

38494936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30674896-C-T

38495088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30675043-G-A

38495104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30675059-C-T

38495121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30675076-C-T

38495244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30675167-C-T

38495469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30675386-A-G

38495503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30675420-A-T

38495907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30675680-A-G

http://identifiers.org/hco/6/GRCh38#38496020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30675775-A-C

38496353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30676069-T-C

38496800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30676184-C-T

38497193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30676639-T-G

38498176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30677768-T-G

38498628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30678176-T-C

http://identifiers.org/hco/6/GRCh38#38498786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30678313-C-A

38498786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30678313-C-G

38499047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30678657-A-G

38499234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30678879-T-C

38499287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30678939-C-T

38499696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30679354-A-G

38500222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30679884-T-C

38500222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30679884-T-G

http://identifiers.org/hco/6/GRCh38#38500555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30680173-C-A

38500626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30680244-T-C

38500634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30680254-C-T

38500993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30680610-A-G

38501082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30680694-T-G

38501138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30680754-T-A

38501590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30680983-G-C

38501707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30681076-G-A

38501827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30681188-T-A

38501901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30681250-T-C

http://identifiers.org/hco/6/GRCh38#38502030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30681369-A-C

38502049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30681388-T-G

http://identifiers.org/hco/6/GRCh38#38502181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30681480-C-A

38502290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30681587-T-C

38502615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30681942-T-A

38502945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30682225-A-G

38503210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30682462-C-T

38503370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30682612-A-G

38503497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30682719-T-C

38503663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30682886-T-C

38503776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30682981-C-T

38504087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30683271-T-C

38504242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30683442-T-C

38504284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30683487-T-C

http://identifiers.org/hco/6/GRCh38#38509691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30683897-A-C

http://identifiers.org/hco/6/GRCh38#38509764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30683951-C-A

38509821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30683988-C-T

38511687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30684535-T-C

38511791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30684638-G-A

38511804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30684653-T-A

38512941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30685398-A-G

38512983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30685439-T-C

38513347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30686165-C-G

38513351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30686169-A-G

http://identifiers.org/hco/6/GRCh38#38513513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30686441-A-C

38513805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30686704-C-T

38514267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30687177-A-G

38514287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30687196-G-A

38514295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30687204-A-G

38514297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30687206-T-C

38514744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30687637-A-G

http://identifiers.org/hco/6/GRCh38#38514766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30687659-A-C

38514943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30687836-G-A

38515290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30688153-G-A

38515444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30688307-G-A

38515601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30688485-T-A

38515875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30688747-A-G

38516352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30689196-G-A

38516572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30689388-G-A

http://identifiers.org/hco/6/GRCh38#38516666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30689485-A-C

38516673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30689492-A-G

38516765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30689583-G-C

38517252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30690077-T-G

38517323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30690149-C-G

38517631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30690390-C-T

http://identifiers.org/hco/6/GRCh38#38518167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30691073-C-A

38518173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30691079-C-T

38518250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30691250-T-A

38518250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30691250-T-C

38518572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30691558-C-T

38518773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30691753-T-A

http://identifiers.org/hco/6/GRCh38#38518839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30691817-A-C

38519034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30691985-T-C

38519116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30692064-C-G

38519128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30692076-A-T

38520497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30693188-T-C

38525075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30694013-C-T

http://identifiers.org/hco/6/GRCh38#38537138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30694144-A-C

38537435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30694387-T-C

38537465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30694397-G-T

38537560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30694458-T-A

38537654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30694557-C-G

38538170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30694966-G-A

38538460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30695244-T-C

38539143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30695867-G-A

38539195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30695938-G-A

38539608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696092-A-G

http://identifiers.org/hco/6/GRCh38#38539784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30696236-A-C

38539984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696429-G-A

38540046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696615-T-G

38540059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696628-A-T

http://identifiers.org/hco/6/GRCh38#38540064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30696633-C-A

38540075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696644-C-T

38540166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696716-G-C

38540259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696779-A-G

38540309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696829-C-T

38540473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30696992-C-T

38540781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30697295-C-T

38540913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30697421-T-C

38541454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30697959-T-C

38541837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698019-G-C

38541837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698019-G-T

38542203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698312-C-T

38542631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698678-T-C

38542728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698765-C-T

38542792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698804-C-T

38542876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698913-C-T

38542884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698921-C-T

38542885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30698922-C-T

38543014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30699047-C-G

38548108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30701852-C-G

38548424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30702152-C-T

38548632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30702345-G-A

38548675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30702384-G-A

38548675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30702384-G-C

38548759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30703090-G-A

38548934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30703258-G-T

38549104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30703426-A-G

38549302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30703630-A-T

38549600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30703903-T-C

http://identifiers.org/hco/6/GRCh38#38551104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30704247-C-A

38551265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30704418-T-C

38551686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30704698-T-C

38551695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30704707-T-C

38551819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30704817-T-C

38551827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30704825-T-C

38551976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30705077-G-A

38551982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30705083-A-G

38552134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30705273-C-T

38552265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30705424-T-C

38552292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30705451-C-G

38553339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30705752-G-T

38553355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30705766-G-C

38553668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30706019-T-C

38554279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30707935-C-T

38554696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30708536-T-C

38554787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30708614-T-C

38554844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30708660-G-A

38554845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30708661-C-T

38554861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30708677-T-C

38554903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30708717-C-T

38554909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30708723-C-T

38555352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30709102-C-T

38555553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30709271-G-A

38556053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30709740-T-A

38556134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30709789-T-C

38556250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30709888-A-G

38556254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30709892-T-C

38564370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30713376-T-A

38564370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30713376-T-C

38564427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30713426-T-C

38566186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30716091-T-C

38566206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30716111-A-G

38566403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30716319-G-A

38566462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30716364-G-T

38566549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30716445-A-G

38566856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30716753-C-T

38566945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30716837-C-T

38567511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30717385-T-A

38567511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30717385-T-C

38567656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30717518-T-C

38567749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30717610-C-T

38567784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30717645-G-C

38567908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30717769-G-A

http://identifiers.org/hco/6/GRCh38#38567932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30717791-A-C

38568090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30717918-T-C

http://identifiers.org/hco/6/GRCh38#38568351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30718141-A-C

http://identifiers.org/hco/6/GRCh38#38569391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30725272-A-C

38569536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30725413-A-G

38569566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30725444-G-C

38569717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30725612-T-C

38569840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30725763-T-C

38569840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30725763-T-G

38570804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30726822-C-T

38570855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30726872-T-G

http://identifiers.org/hco/6/GRCh38#38571152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30727167-C-A

38571256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30727267-T-C

38571478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30727492-G-A

38571506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30727520-G-C

38571544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30727557-C-T

38571624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30727635-T-C

http://identifiers.org/hco/6/GRCh38#38571633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30727644-A-C

38572175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30727767-A-G

38572314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30727900-G-A

38572429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30728039-T-G

38572489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30728099-T-C

38572660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30728259-A-G

38572785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30728341-G-A

38572897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30728445-G-A

38572943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30728488-A-T

38574268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30728876-G-A

38574606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30729196-T-A

38574671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30729261-C-T

38575402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30729848-C-G

38576006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30731075-A-G

38576222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30731301-G-A

38576651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30731692-T-C

38576669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30731731-C-T

38576774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30731828-T-C

38576774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30731828-T-G

http://identifiers.org/hco/6/GRCh38#38576813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30731868-A-C

38577217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732207-T-C

38577251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732220-T-G

38577330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732275-T-C

38577433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732368-A-G

http://identifiers.org/hco/6/GRCh38#38577493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30732429-C-A

38577493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732429-C-T

38577742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732672-A-T

38577771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732691-A-G

38577801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732719-G-A

38577801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732719-G-T

38578107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30732973-A-G

38578196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30733064-G-A

38578215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30733089-G-A

38578215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30733089-G-C

38578215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30733089-G-T

38579058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30733920-T-C

38579061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30733923-G-A

38579188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734280-G-A

38579188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734280-G-T

http://identifiers.org/hco/6/GRCh38#38579200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30734292-C-A

38579200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30734292-C-G

38579201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734293-T-C

38579259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734350-G-C

38579266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734357-T-C

38579292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734383-C-T

38579333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734420-C-T

38579388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734461-G-C

38579434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734501-T-C

38579531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734573-C-G

38579780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734881-G-A

38579780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21228
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30734881-G-C