34889293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5 prime UTR variant
orthologous variants: 28128328-T-A

34889293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5 prime UTR variant
orthologous variants: 28128328-T-C

34889387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5 prime UTR variant
orthologous variants: 28128420-G-A

34889387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5 prime UTR variant
orthologous variants: 28128420-G-T

34889456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28128489-G-A

34889456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28128489-G-C

34889456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28128489-G-T

34889516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28128546-T-C

34889516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28128546-T-G

http://identifiers.org/hco/6/GRCh38#34889618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28128635-C-A

34889618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28128635-C-T

34889877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28128792-A-G

34890502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28129089-T-C

34890735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28129315-G-C

34890816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28129391-C-G

34890816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28129391-C-T

34890908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28129482-G-T

http://identifiers.org/hco/6/GRCh38#34890933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28129507-A-C

34890933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28129507-A-G

34890954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28129534-A-T

34891044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130011-A-G

34891044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130011-A-T

34891286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130224-A-G

34891950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130772-G-A

34891958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130778-G-A

34892042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130851-G-A

34892126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130916-G-A

34892168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130960-A-G

34892188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28130980-C-G

34892277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28131135-A-G

34892298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28131178-T-C

34892302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28131315-T-C

34892526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28131532-G-A

34893316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28132864-T-G

34893382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28132926-C-T

34893639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28133223-G-T

http://identifiers.org/hco/6/GRCh38#34893724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28133307-A-C

http://identifiers.org/hco/6/GRCh38#34893894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28133457-A-C

34894035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28133565-T-C

34894056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28133586-G-T

34894279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28133793-T-G

34895683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28134622-A-G

34897633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28136042-C-T

http://identifiers.org/hco/6/GRCh38#34898146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28136513-C-A

http://identifiers.org/hco/6/GRCh38#34900095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28140162-C-A

34900132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28140185-C-T

34900818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28140586-T-C

34903116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28142273-A-G

34903116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28142273-A-T

34908543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28144631-G-T

34908624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28144731-C-T

34908684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28144793-G-A

34908760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28144861-C-T

34909035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28145227-T-C

34909111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28145278-C-T

34909483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28145580-C-T

34909810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28145892-T-C

34910139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28146134-C-T

34910970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28146272-T-A

34910972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28146274-G-A

34911274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28146629-C-T

34911458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28146849-G-A

34911458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28146849-G-C

34911702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28147707-C-T

34911833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28147826-T-G

34912186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28148189-T-C

34912323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28148300-A-G

34912704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28148829-G-A

34914629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28150731-T-G

34914868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28150914-G-A

34914868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28150914-G-T

34916921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28153599-A-T

34917111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28154550-C-T

34917341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28154760-C-T

34917429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28154850-A-T

34917996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28156128-T-G

34918202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28156301-T-G

34918381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28156406-C-T

34918517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28156530-G-C

34918773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28156763-G-A

34918773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28156763-G-T

34918800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28156788-A-T

34919293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28157054-A-G

34919401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28157157-C-T

34926604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28159292-G-A

34926604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28159292-G-C

34926739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28159440-T-G

34927217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28159842-G-T

34927330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28159934-A-G

34927418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28160021-A-T

34927501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28160284-G-A

34927791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28160565-T-C

34927881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28160630-C-T

34927940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28160687-G-T

34928047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28160790-A-T

34928059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28160802-T-G

34933719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28164294-C-T

34933728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28164303-A-G

34933994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28164655-G-T

34934624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28164916-C-T

34934625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28164917-G-A

34934784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28165093-A-G

34934975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28165230-T-G

34934996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28165251-T-G

34935408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28165456-G-A

34935408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28165456-G-C

34935551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28165614-A-G

34935590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28165653-A-G

34936646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28167330-C-T

34936764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28167447-T-G

34939907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28173910-C-T

34939933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28173938-G-A

34940068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28174051-T-A

34940180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28174156-G-A

34940266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28174226-G-C

34940390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28174347-G-A

34940409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28174366-C-G

34940492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28174429-C-T

http://identifiers.org/hco/6/GRCh38#34941366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28174912-A-C

http://identifiers.org/hco/6/GRCh38#34946973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28178927-A-C

34946973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28178927-A-G

34946986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28178940-G-A

http://identifiers.org/hco/6/GRCh38#34947624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28179197-C-A

34947625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28179198-A-G

34948401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28179817-G-T

34949166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28180811-A-G

34949748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28182653-A-T

34949992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28182850-C-T

34951831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28183506-T-C

34953244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28185471-C-T

34953797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28185867-G-T

34954001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28186043-G-A

http://identifiers.org/hco/6/GRCh38#34954013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28186055-A-C

34960600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28188089-G-T

http://identifiers.org/hco/6/GRCh38#34960649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28188139-A-C

34960649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28188139-A-G

34960923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28188340-A-G

34966826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28193502-C-T

34966905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28193566-A-G

34966954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28193619-A-G

34967100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28193768-T-C

34967180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28193834-T-G

34967251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28193891-G-A

34968296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28194424-C-G

34968315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28194443-G-A

34968354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28194480-T-A

34969065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28194993-G-A

34969099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195027-A-G

34969146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195073-G-A

34969153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195080-G-A

34969704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195275-G-A

34969872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195426-G-T

http://identifiers.org/hco/6/GRCh38#34969883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28195437-C-A

34969883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195437-C-T

34969920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195456-G-A

34969920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28195456-G-T

34970040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous_variant, undefined
orthologous variants: 28195565-T-C

34971302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28196372-G-A

34972206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28197072-G-A

34972312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28197163-G-A

34972496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28197320-G-A

http://identifiers.org/hco/6/GRCh38#34972505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28197326-C-A

34972505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28197326-C-T

34976446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28199526-C-G

34976472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28199557-G-A

34976472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28199557-G-T

34976616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28199654-T-C

34976823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28199800-G-T

34979807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28202471-C-T

34980367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28202887-A-G

34980369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28202889-C-T

34980407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28202925-G-A

34980716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28203187-G-A

34980751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28203207-A-G

34981064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28203484-A-G

34981157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28203576-T-A

34981538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28203904-G-A

34981538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28203904-G-T

34981740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28204090-A-G

34981824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28204174-A-G

http://identifiers.org/hco/6/GRCh38#34982027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28204376-C-A

34982027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28204376-C-G

34982105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28204445-A-G

34982105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28204445-A-T

34982106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28204446-T-C

34982124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28204470-T-C

34982136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28204482-A-G

34982136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28204482-A-T

http://identifiers.org/hco/6/GRCh38#34982623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28204929-A-C

34982623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28204929-A-G

http://identifiers.org/hco/6/GRCh38#34982725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28205201-C-A

34982725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205201-C-G

34982725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205201-C-T

34982969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205381-T-C

34982970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205382-G-A

34982970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205382-G-C

34982970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205382-G-T

34982999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205411-G-A

34983013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205425-G-C

34983013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205425-G-T

34983077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205487-G-A

34983077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205487-G-C

http://identifiers.org/hco/6/GRCh38#34983417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28205812-A-C

34983467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205840-G-A

34983502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205875-A-T

34983554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205918-A-G

34983614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28205972-G-T

34983642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28206000-C-G

34984850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28207456-G-C

34984860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28207466-G-C

34984860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28207466-G-T

34985146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28207758-T-G

34985152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28207764-C-T

34985212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28207824-A-G

34985373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28208036-G-A

34985373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28208036-G-T

34985546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28208177-G-A

34985546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28208177-G-C

http://identifiers.org/hco/6/GRCh38#34985648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28208291-C-A

34986477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28208682-C-T

34986934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, undefined
orthologous variants: 28208929-G-A

34987118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28209042-T-C

34987298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28209173-C-T

34987590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28209385-T-G

34987866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28209592-G-T

34988054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28209735-G-C

http://identifiers.org/hco/6/GRCh38#34988273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28209980-C-A

34988273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28209980-C-G

34988370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28210117-G-A

34989260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: missense variant
orthologous variants: 28210318-G-A

34989260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: missense variant
orthologous variants: 28210318-G-T

34989324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28210382-G-A

34989341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28210396-C-T

34991903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28212844-C-G

34992491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28213338-T-A

34992565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28213407-G-A

34993261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28213975-C-T

34993541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28214111-T-C

34993596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28214162-G-A

34993764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28214315-T-C

http://identifiers.org/hco/6/GRCh38#34994232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28214852-A-C

34994232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28214852-A-T

34994246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28214866-G-A

34994246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28214866-G-T

34994298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28214904-T-G

34994382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28214988-A-G

34994437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215043-A-G

34994559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215078-G-C

34994559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215078-G-T

34994636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215157-T-A

34994636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215157-T-C

34994710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215254-A-G

34994870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215355-C-T

34994888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28215373-C-T

34998058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28217033-A-G

35008669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28219689-C-T

35008838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28219869-T-C

35008880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28219910-C-T

35009135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28220141-T-C

35009281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28220244-G-A

35010576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28220720-G-A

35010623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28220753-G-C

35011341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221421-A-G

35011411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221491-G-C

35011727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221753-T-G

35011729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221755-C-T

35011762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221784-G-C

35011834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221851-T-G

35011858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221876-G-T

35011889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28221906-A-G

35012108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28222083-A-G

35012353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28222300-G-A

35012577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28222466-G-T

http://identifiers.org/hco/6/GRCh38#35012621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28222510-A-C

35012747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28222630-T-C

35012864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28222738-T-G

35014538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28224564-G-A

35015051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28224998-A-G

35015816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28225322-C-T

35015844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28225342-G-A

35015844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28225342-G-C

http://identifiers.org/hco/6/GRCh38#35016124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28225529-C-A

35016124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28225529-C-T

35016244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28225640-A-G

35016753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28226154-G-A

35016814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28226213-A-G

35016988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28226393-G-A

35017154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28226530-G-A

35017493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 28226843-A-G

35017632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 28226982-C-G

35017696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28227043-G-A

35017820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: missense variant
orthologous variants: 28227167-C-T

35017834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28227181-T-C

http://identifiers.org/hco/6/GRCh38#35018092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28227439-C-A

35018092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227439-C-T

35018109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227457-A-G

35018160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227507-A-G

35018160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227507-A-T

35018172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227514-T-A

35018172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227514-T-G

35018465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227763-A-G

35019082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28227981-A-G

35019104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28228014-G-C

35019914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28228591-G-A

35020974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28229543-G-A

35022398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28230222-G-A

http://identifiers.org/hco/6/GRCh38#35022576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28230396-A-C

35022777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28230534-A-G

35024941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28232537-C-T

35024957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28232543-T-C

35026448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28233990-G-C

35026546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28234063-C-T

35026572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28234080-G-A

35026572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28234080-G-C

35026677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28234144-A-G

35026921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28234340-C-G

http://identifiers.org/hco/6/GRCh38#35027052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28234456-C-A

35027503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28234899-C-T

35027546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28234936-T-C

http://identifiers.org/hco/6/GRCh38#35027993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28235247-C-A

35029914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28236828-A-G

35029914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28236828-A-T

35029936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28236850-G-A

35029986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28236893-A-G

35030276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28237183-C-T

35030489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28237372-T-G

35031567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28238259-G-A

35034889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28241008-C-G

35035036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28241147-C-T

http://identifiers.org/hco/6/GRCh38#35035093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28241220-A-C

35035102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28241230-G-A

35035870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28241853-T-C

http://identifiers.org/hco/6/GRCh38#35036930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28242639-A-C

35037459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28243071-G-A

35037635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28243170-A-G

35037973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28243467-G-A

35038248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28243725-G-T

35040293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28244544-G-A

35040800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28244886-C-T

35041543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28245459-C-G

35041689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28245560-T-C

http://identifiers.org/hco/6/GRCh38#35042032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28245800-A-C

35042032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28245800-A-G

35042446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28246088-C-G

35042446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28246088-C-T

35042525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28246161-G-A

35042569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28246196-C-G

35042569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28246196-C-T

35042943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28246720-G-A

35043015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28246998-A-G

35043092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247063-T-G

35043199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247144-A-G

35043232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247177-A-G

35043342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247292-G-C

35043424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247332-C-G

35043480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247386-C-T

35043488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247394-T-C

35043594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247485-A-G

35043604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247494-T-C

35043711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247604-A-G

35043792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247681-C-T

35044010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28247889-T-C

35045497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28249301-T-C

35045548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28249342-A-G

35045913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28249601-C-T

35046083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28249761-T-C

35046184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28249863-G-A

35046271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28249942-C-T

35046625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28250269-A-G

35046660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28250304-G-A

35046889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28250522-A-G

35047007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28250663-C-G

35047083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28250728-A-G

35047158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28250784-T-G

35047332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28250910-A-T

35047634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28251162-T-C

35047806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28251317-T-C

35047840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28251353-G-A

35048217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28251873-T-C

35048475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28252118-C-G

35048620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28252288-G-A

35048624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28252292-G-T

35048927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28252532-G-T

35049318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28252968-A-G

35049649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28253269-G-A

35049649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28253269-G-T

35050034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28253620-T-G

35050069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28253635-G-A

35050205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28253741-G-T

35053412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28256562-T-C

35053510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28256644-G-A

35053616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28256745-A-G

35054437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28257364-G-A

35054437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28257364-G-C

35054445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28257372-T-C

35054453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28257380-T-A

35054725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28257654-C-T

35054914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28257805-T-C

35054986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28257831-G-A

35055714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28258177-C-T

35055751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28258214-C-G

35055751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28258214-C-T

35055924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28258360-G-A

35057026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28258875-C-T

http://identifiers.org/hco/6/GRCh38#35057305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28259047-C-A

35057305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28259047-C-T

35057405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28259114-A-G

35057681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28259329-G-A

35057905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28259470-A-G

35058173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28259710-G-A

35058173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28259710-G-T

http://identifiers.org/hco/6/GRCh38#35058186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28259723-C-A

35058186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28259723-C-T

35058212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28259746-T-A

35058212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28259746-T-C

http://identifiers.org/hco/6/GRCh38#35058287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28259800-C-A

35058287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28259800-C-T

35058295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28259810-C-T

http://identifiers.org/hco/6/GRCh38#35058296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28259811-C-A

35058296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28259811-C-T

35058678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 28260169-G-T

35058804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260290-C-T

35058968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260447-C-T

35059021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260513-G-A

35059021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260513-G-T

35059298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260760-T-G

35059365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260802-A-T

35059497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260917-G-A

35059497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260917-G-C

35059547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260960-C-T

35059565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28260978-G-A

35059611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28261024-T-C

35059660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28261073-G-A

http://identifiers.org/hco/6/GRCh38#35059744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28261156-C-A

35059744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28261156-C-T

35060067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 28261464-T-C

35060123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 28261520-G-A

35060123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 28261520-G-T

35060208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 28261605-T-G

35060238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28261635-C-T

35060289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28261686-T-G

35060354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28261728-G-T

35060368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28261742-G-A

35060368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28261742-G-T

35060388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28261760-T-C

35060432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28261804-A-T

35060958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28262314-C-T

35062099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28263369-G-A

35062146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28263398-G-A

35062281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28263520-T-A

35062281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28263520-T-C

35063221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28264356-C-T

http://identifiers.org/hco/6/GRCh38#35064570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28264824-C-A

35064570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28264824-C-T

35064819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28265077-T-A

35074841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28267697-T-G

35075014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28267834-G-A

35077722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269014-G-C

35077950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269177-C-G

35077950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269177-C-T

35078013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269230-C-T

35078467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269462-G-T

http://identifiers.org/hco/6/GRCh38#35078486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28269481-C-A

35078486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269481-C-T

35078530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269517-G-A

35078530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269517-G-T

35078599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28269581-C-T

35078675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269694-G-A

35078675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269694-G-C

http://identifiers.org/hco/6/GRCh38#35078758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28269867-C-A

35078758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269867-C-T

35078805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269934-G-C

35078805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28269934-G-T

35078997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28270156-G-A

35079171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28270286-C-T

35079507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28270462-G-A

35079668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 28270623-T-C

35079815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28270689-A-G

35079883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28270761-G-A

35080072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28270913-G-A

35080247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271041-A-G

35080418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271151-C-G

35080418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271151-C-T

35080666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271344-T-A

35080666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271344-T-C

35080828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271469-G-A

35080921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271560-G-A

35080931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271570-G-A

35080931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28271570-G-T

35081058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: missense variant
orthologous variants: 28271677-C-T

35081059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28271678-G-A

35081059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28271678-G-T

http://identifiers.org/hco/6/GRCh38#35081113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28271732-C-A

35081113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28271732-C-T

35081122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28271741-T-C

35081126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: missense variant
orthologous variants: 28271745-G-A

35081212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271789-G-A

35081212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271789-G-T

35081218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271795-G-A

35081218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271795-G-T

35081219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271796-G-A

35081219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271796-G-T

http://identifiers.org/hco/6/GRCh38#35081226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28271803-A-C

35081227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271804-G-A

35081227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271804-G-T

35081233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271810-C-T

35081266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271821-G-A

35081266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271821-G-T

35081355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28271884-C-T

35081625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28272095-A-G

35081914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28272366-G-C

35082174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28272585-C-T

35082178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28272589-G-A

35082320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28272666-G-A

35082711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28272884-G-A

35082802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: missense variant
orthologous variants: 28272975-G-A

35082897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273056-G-A

35083013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273134-G-A

35083013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273134-G-C

35083013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273134-G-T

http://identifiers.org/hco/6/GRCh38#35083016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28273137-C-A

35083016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273137-C-T

35083065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273177-A-G

35083065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273177-A-T

35083081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273193-G-A

35083384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273613-G-A

35083384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28273613-G-C

35083425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28273652-G-A

35083988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28276178-G-T

35084056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28276239-T-C

35084192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28276372-T-C

35085694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28277202-G-T

35085720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28277226-G-C

35085724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28277230-C-T

35085924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28277422-G-A

35085924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: synonymous variant
orthologous variants: 28277422-G-T

35085983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28277459-G-T

http://identifiers.org/hco/6/GRCh38#35086079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28277552-C-A

35086079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28277552-C-T

35086275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 28277727-G-A

35086462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28277911-C-T

http://identifiers.org/hco/6/GRCh38#35087172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28278474-C-A

35088433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28279392-G-T

35088731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28279653-A-G

35088892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28279804-A-T

35089197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28279978-T-C

35089197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28279978-T-G

http://identifiers.org/hco/6/GRCh38#35089198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28279979-C-A

35089199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28279980-A-G

35089274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28279999-T-C

http://identifiers.org/hco/6/GRCh38#35089445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28280112-C-A

35089446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280113-A-G

http://identifiers.org/hco/6/GRCh38#35089654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28280305-C-A

35089654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280305-C-T

http://identifiers.org/hco/6/GRCh38#35089662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28280313-C-A

35089662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280313-C-T

35089663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280314-T-C

35089669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280320-G-A

35089669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280320-G-T

35089826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280466-G-A

35089855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280523-G-A

35089855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280523-G-T

http://identifiers.org/hco/6/GRCh38#35089877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28280545-C-A

35090041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280650-A-G

35090083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280678-G-A

35090083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280678-G-C

35090126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280718-A-G

35090404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280905-C-G

35090404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280905-C-T

35090405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280906-G-A

35090405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28280906-G-T

35090640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28281095-T-C

35090702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28281132-G-T

http://identifiers.org/hco/6/GRCh38#35090798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28281201-C-A

35090845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28281251-C-T

35090846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28281252-A-G

http://identifiers.org/hco/6/GRCh38#35090849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28281255-C-A

35090849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28281255-C-G

35090849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28281255-C-T

35091071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28281430-C-T

35091464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28281797-G-T

35091486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: 28281819-G-T

http://identifiers.org/hco/6/GRCh38#35091559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28281878-C-A