38875983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 80597644-G-A

38875983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 80597644-G-T

http://identifiers.org/hco/2/GRCh38#38876161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80597791-C-A

38876161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80597791-C-T

38876214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80597831-G-T

http://identifiers.org/hco/2/GRCh38#38876246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80597861-C-A

38876246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80597861-C-T

38876279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80597884-T-A

38876280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80597885-G-T

38876365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80597943-C-T

38876574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599188-G-C

38876574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599188-G-T

38876595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599209-G-A

38876595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599209-G-C

38876660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599262-A-G

38879893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599623-A-G

38879893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599623-A-T

http://identifiers.org/hco/2/GRCh38#38880040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80599737-C-A

38880040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599737-C-T

http://identifiers.org/hco/2/GRCh38#38880179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80599757-C-A

38880243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599821-T-C

38880243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80599821-T-G

38880373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80601661-G-C

38880373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80601661-G-T

38880543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80601810-T-C

38880643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80601942-T-C

38880643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80601942-T-G

38880725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80602024-A-G

38880795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80602106-T-C

38881275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80602801-A-G

http://identifiers.org/hco/2/GRCh38#38881400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80602902-C-A

38881400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80602902-C-G

38881400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80602902-C-T

38881408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80602910-T-C

38881408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80602910-T-G

38881583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603083-G-A

38881583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603083-G-C

http://identifiers.org/hco/2/GRCh38#38881612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80603110-C-A

38881612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603110-C-G

http://identifiers.org/hco/2/GRCh38#38881679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80603183-C-A

38881679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603183-C-G

38881679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603183-C-T

http://identifiers.org/hco/2/GRCh38#38881711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80603216-A-C

38881803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603252-A-G

38881865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603328-G-C

38881930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603383-C-G

38881930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80603383-C-T

http://identifiers.org/hco/2/GRCh38#38882130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80604419-C-A

38882130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80604419-C-T

http://identifiers.org/hco/2/GRCh38#38882276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80604536-A-C

38882276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80604536-A-G

38882276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80604536-A-T

38882277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80604537-T-A

38882277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80604537-T-G

38882302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80604561-A-G

38882330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80604591-T-C

38882442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 80604712-T-A

38882442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 80604712-T-C

http://identifiers.org/hco/2/GRCh38#38882577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80604841-C-A

38882581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 80604845-A-T

http://identifiers.org/hco/2/GRCh38#38882583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80604847-C-A

38882583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 80604847-C-G

38882616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 80604875-A-G

38882616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 80604875-A-T

http://identifiers.org/hco/2/GRCh38#38882633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80604889-A-C

38889080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614047-C-T

38889209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614173-T-C

38889226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614191-G-A

38889477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614457-A-G

38889607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614582-A-T

38889608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614583-A-T

38889777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614750-T-G

38889805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614765-T-C

38889831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80614791-C-G

38889902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80614861-T-A

http://identifiers.org/hco/2/GRCh38#38889969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80614928-C-A

38890085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615032-T-C

38890118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615065-T-C

38890225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615167-C-T

38890387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615333-A-G

38890387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615333-A-T

38890597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615562-G-A

38890765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615726-T-C

38891011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80615959-C-T

38891115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616046-G-A

38891115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616046-G-T

http://identifiers.org/hco/2/GRCh38#38891134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80616069-A-C

38891134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616069-A-G

38891134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616069-A-T

38891419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616444-C-T

38891497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616538-G-A

38891572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616665-C-T

38891762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80616896-A-G

38892148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80617246-G-T

38892748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618187-A-G

38892792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618232-C-G

38892837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618272-G-A

38892943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618375-A-G

38893520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618606-T-A

38893529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618612-T-A

38893561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618626-A-G

38893644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618690-T-C

38893725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80618780-T-C

http://identifiers.org/hco/2/GRCh38#38894384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80619238-C-A

38894384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80619238-C-T

http://identifiers.org/hco/2/GRCh38#38894525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80619358-C-A

38894686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80619507-A-G

38894749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80619558-A-G

38895001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80619829-G-A

38895051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80619883-G-T

38895107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80619927-C-T

38895265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80620104-T-A

38895265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80620104-T-G

38895322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80620124-A-T

38895386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80620214-A-G

http://identifiers.org/hco/2/GRCh38#38896116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80620829-A-C

38897640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80622560-C-T

38897717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80622625-T-A

38898368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80623379-C-T

38898556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80623531-A-G

38898556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80623531-A-T

38898559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80623533-A-G

38898659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80623629-T-G

38898696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80623661-T-C

38898763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80623728-T-C

38899163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80624234-C-G

http://identifiers.org/hco/2/GRCh38#38899478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80624826-A-C

38899579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80624916-G-A

38899580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80624917-C-T

38899581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80624918-G-A

38899582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80624919-T-C

38899587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80624924-C-G

38899587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80624924-C-T

38899699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625063-T-C

38899776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625140-G-A

38899837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625211-G-T

38899914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625251-C-G

38899941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625278-C-T

38901070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625803-A-G

http://identifiers.org/hco/2/GRCh38#38901076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80625809-C-A

38901076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625809-C-T

38901281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625870-G-A

38901357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625928-G-A

38901419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625987-G-C

38901433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80625989-C-T

38901538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80626095-C-G

38901538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80626095-C-T

38901636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80626197-C-T

38901641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80626202-T-C

http://identifiers.org/hco/2/GRCh38#38901796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80626372-A-C

38901798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80626374-C-T

38902842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80626724-G-A

38902917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80626749-A-G

38903237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627083-A-G

38903318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627254-T-G

38903328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627264-C-T

38903359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627293-A-G

38903359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627293-A-T

38903401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627319-A-G

38903523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627459-T-A

38903524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627460-A-G

38903527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627463-G-A

38903546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80627480-A-G

http://identifiers.org/hco/2/GRCh38#38903742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80627662-C-A

38904277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80628104-G-T

38904281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80628108-G-C

38906226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80628899-A-G

http://identifiers.org/hco/2/GRCh38#38906267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80628938-A-C

38906303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80628973-T-C

38907241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80630358-A-G

http://identifiers.org/hco/2/GRCh38#38907424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80630518-C-A

38907424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80630518-C-G

38907522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80630616-G-C

38907528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80630621-C-T

38907666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80630773-G-T

38908092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80630979-T-G

38908146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631010-T-C

38908250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631113-A-G

38908262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631123-A-G

38908262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631123-A-T

38908343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631199-G-T

38908371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631227-C-T

38908457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631301-C-T

38908624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631443-A-G

38908638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631458-C-T

38908725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631545-C-G

38908725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631545-C-T

38908772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631589-G-C

38908883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631696-A-G

38908896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80631709-G-A

http://identifiers.org/hco/2/GRCh38#38908898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80631726-C-A

38909970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80632439-G-A

38909970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80632439-G-T

http://identifiers.org/hco/2/GRCh38#38910025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80632477-C-A

38910025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80632477-C-G

38910824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80633519-T-C

38910852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80633547-C-G

38910947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80633630-C-G

http://identifiers.org/hco/2/GRCh38#38910989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80633668-C-A

38911073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80633731-G-A

38911127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80633781-T-A

38911197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80633855-C-T

38911237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80633896-A-G

http://identifiers.org/hco/2/GRCh38#38911517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80634173-C-A

38911517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80634173-C-T

38911518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80634174-G-A

38911695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80634350-C-G

38911695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80634350-C-T

http://identifiers.org/hco/2/GRCh38#38911736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80634392-C-A

38912058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80635460-A-G

38912109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80635519-C-T

38912213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80635619-G-A

38912213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80635619-G-T

38912403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80635867-C-G

38916140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80641543-C-G

38918706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80641965-T-C

38918706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80641965-T-G

38919208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642518-A-G

38919218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642528-T-G

38919253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642562-G-A

38919253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642562-G-C

38919253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642562-G-T

38919294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642599-T-A

38919294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642599-T-G

http://identifiers.org/hco/2/GRCh38#38919343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80642646-C-A

38919354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642653-A-T

38919380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 80642679-T-C

38919404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 80642703-T-C

38919463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80642762-A-G

38919499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642792-A-G

38919529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80642822-T-C

38920177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80643339-A-G

38920196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80643358-A-G

http://identifiers.org/hco/2/GRCh38#38920243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80643421-C-A

38920345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80643515-C-T

38920910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80643716-G-A

38920940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80643750-G-A

38921052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644374-A-G

38921158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644482-A-G

38921224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644549-G-A

38921224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644549-G-T

http://identifiers.org/hco/2/GRCh38#38921225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644550-C-A

38921225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644550-C-G

38921282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644606-A-G

http://identifiers.org/hco/2/GRCh38#38921289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644613-A-C

http://identifiers.org/hco/2/GRCh38#38921366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644690-C-A

38921366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 80644690-C-G

38921366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 80644690-C-T

http://identifiers.org/hco/2/GRCh38#38921367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644691-C-A

38921367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 80644691-C-G

38921370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 80644694-G-T

38921488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644807-G-T

38921509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80644826-A-G

38922109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80645577-A-T

38922238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80645691-C-T

38922514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646441-C-T

38922515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646442-G-A

38922537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646462-G-T

http://identifiers.org/hco/2/GRCh38#38922611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80646531-C-A

38922653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646573-T-C

38922679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646599-T-C

38922727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646650-T-C

38922742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646665-T-C

38922904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80646828-T-A

38923092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647023-C-T

38923125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647060-G-T

38923168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647107-G-T

38923206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647130-G-A

38923224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647144-G-A

38923225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647145-A-T

http://identifiers.org/hco/2/GRCh38#38923284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80647193-C-A

38923284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647193-C-G

38923294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647203-C-T

38923348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647225-A-G

38923362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647239-A-T

38923448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80647327-C-G

38925408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80649699-A-G

38925408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80649699-A-T

38925450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80649738-A-T

38925533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80649830-G-C

38925602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80649897-G-T

38925793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80650269-G-C

38925817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80650292-C-T

38925931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80650408-G-T

38926084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80650553-A-G

38926103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80651066-G-A

38926164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 80651118-G-A

http://identifiers.org/hco/2/GRCh38#38926166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80651120-C-A

38926167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 80651121-C-T

38926306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80651259-C-T

38926314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80651267-A-G

38926353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80651298-G-A

38926476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80651417-T-C

38927182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80652575-A-T

38927332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80652724-A-G

38927370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80652771-T-C

38927644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80652971-C-T

38927657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80652983-C-G

38927691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653005-G-A

38927691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653005-G-C

38927773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653068-C-T

38927799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653094-T-G

38927909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653191-G-A

38928100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653382-A-G

38928265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653567-T-A

38928356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80653607-C-T

38928569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80654060-C-T

38928645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80654301-A-T

38928664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80654313-T-C

38928669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80654318-G-T

38928682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80654331-T-A

38928717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80654359-G-T