136006660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25945666-A-G

136006831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25945880-A-G

136006873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25945920-T-C

http://identifiers.org/hco/9/GRCh38#136006964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25946027-C-A

http://identifiers.org/hco/9/GRCh38#136007287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#25946324-C-A

136007861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25946626-T-C

136007933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25946692-C-T

136008078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25946811-G-T

136008361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947080-G-T

136008587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947289-C-T

136008589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947290-G-T

136008600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947301-T-A

136008600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947301-T-G

http://identifiers.org/hco/9/GRCh38#136008934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25947639-C-A

136008962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947667-G-A

136008962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947667-G-T

136009103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947806-G-A

136009103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947806-G-T

136009197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947930-G-A

136009197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25947930-G-T

136009515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948209-G-T

http://identifiers.org/hco/9/GRCh38#136009519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25948213-C-A

136009519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948213-C-T

136009529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948222-T-C

136009766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948402-C-T

136009911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948479-G-A

136009911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948479-G-T

http://identifiers.org/hco/9/GRCh38#136010133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25948649-C-A

136010291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948779-T-A

136010291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948779-T-C

http://identifiers.org/hco/9/GRCh38#136010293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25948781-C-A

136010293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948781-C-T

http://identifiers.org/hco/9/GRCh38#136010341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25948806-A-C

136010341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948806-A-G

136010341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948806-A-T

136010344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948809-G-A

136010344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948809-G-T

136010401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948845-T-C

136010406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25948850-A-G

http://identifiers.org/hco/9/GRCh38#136010684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949098-C-A

http://identifiers.org/hco/9/GRCh38#136010708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949122-C-A

http://identifiers.org/hco/9/GRCh38#136010738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949147-C-A

136010858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949223-G-A

136010858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949223-G-C

136010858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949223-G-T

http://identifiers.org/hco/9/GRCh38#136010880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949245-C-A

136010880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949245-C-T

136010882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949247-A-G

http://identifiers.org/hco/9/GRCh38#136010919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949335-A-C

136010919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949335-A-T

http://identifiers.org/hco/9/GRCh38#136010945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949388-C-A

136010945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949388-C-T

http://identifiers.org/hco/9/GRCh38#136010946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949389-A-C

136010946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949389-A-G

136010946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949389-A-T

136010982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949451-G-A

136010982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949451-G-T

136010986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949455-G-A

136010986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949455-G-T

http://identifiers.org/hco/9/GRCh38#136011008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25949469-C-A

136011008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949469-C-T

136011081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949546-G-A

136011081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949546-G-T

136011353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949810-T-G

136011357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: 3 prime UTR variant
orthologous variants: 25949814-T-G

http://identifiers.org/hco/9/GRCh38#136011770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25950231-C-A

136011770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25950231-C-G

136011770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25950231-C-T

136011823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25950284-G-A

136011823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25950284-G-T

http://identifiers.org/hco/9/GRCh38#136011876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25950337-C-A

136011876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25950337-C-G

136011876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25950337-C-T

http://identifiers.org/hco/9/GRCh38#136012076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25950536-C-A

136012076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25950536-C-G

136012076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25950536-C-T

136012844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951212-C-T

136013064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951432-T-C

http://identifiers.org/hco/9/GRCh38#136013065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25951433-C-A

136013065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951433-C-T

http://identifiers.org/hco/9/GRCh38#136013074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25951442-C-A

136013074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951442-C-T

136013099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951463-A-G

136013141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951501-G-A

136013141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951501-G-C

136013141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951501-G-T

http://identifiers.org/hco/9/GRCh38#136013169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25951550-C-A

136013169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951550-C-T

http://identifiers.org/hco/9/GRCh38#136013177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25951559-C-A

136013177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951559-C-G

136013177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951559-C-T

136013306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951692-G-A

136013385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951751-G-A

136013385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951751-G-T

136013418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951797-G-A

136013418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951797-G-T

136013427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951807-T-A

136013427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951807-T-C

136013450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951818-C-T

136013551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951912-G-A

136013564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951925-G-A

136013609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25951971-A-G

http://identifiers.org/hco/9/GRCh38#136013779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25952135-C-A

136013807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952164-G-T

http://identifiers.org/hco/9/GRCh38#136014050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25952383-A-C

136014050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952383-A-G

136014050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952383-A-T

136014051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952384-G-A

136014051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952384-G-C

136014051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952384-G-T

136014052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952385-G-A

136014052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952385-G-C

136014052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25952385-G-T

136015470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25953599-T-C

136015555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25953707-G-A

136015840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25954094-C-G

136015947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25954155-C-T

136016119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25954325-A-G

136016119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25954325-A-T

136016193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25954411-G-A

136016193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25954411-G-T

136016439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25954639-C-G

136016483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25954687-C-T

136016579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25954735-T-A

136016579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25954735-T-C

136016608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25954761-T-C

136016610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25954763-C-T

http://identifiers.org/hco/9/GRCh38#136016823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25954975-C-A

136016847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25955038-G-C

136017379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25955526-C-T

136017404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25955550-G-A

136017411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25955557-T-C

http://identifiers.org/hco/9/GRCh38#136017480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25955618-A-C

136017483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25955621-A-G

http://identifiers.org/hco/9/GRCh38#136017526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25955661-A-C

136018024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25955895-G-A

http://identifiers.org/hco/9/GRCh38#136018309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25956125-C-A

136018476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25956306-T-C

136018638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25956464-C-T

http://identifiers.org/hco/9/GRCh38#136019194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25957052-C-A

136019194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25957052-C-T

136019223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25957080-C-T

http://identifiers.org/hco/9/GRCh38#136019252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25957106-C-A

136019315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25957164-G-C

136019322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25957171-G-A

136019322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25957171-G-T

136019363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25957240-A-T

136019391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25957265-G-C

http://identifiers.org/hco/9/GRCh38#136019602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25957437-C-A

136019602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25957437-C-T

136044995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25976382-G-A

136046950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25977957-G-A

136046950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25977957-G-C

136047095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25978098-G-A

136047157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 25978143-C-T

136047461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25978403-T-C

http://identifiers.org/hco/9/GRCh38#136047492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25978433-C-A

136047507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25978449-C-T

136047700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25978637-C-T

136049629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 25979546-G-A

136049629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 25979546-G-C

136049629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 25979546-G-T

136049814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25979733-G-A

136049997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25979919-A-G

136049997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25979919-A-T

http://identifiers.org/hco/9/GRCh38#136050106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25980019-C-A

136050106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25980019-C-G

136050106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25980019-C-T

http://identifiers.org/hco/9/GRCh38#136050225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25980138-C-A

136050225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25980138-C-G

136050225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25980138-C-T

136050228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25980141-G-A

136050228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25980141-G-C

136050228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25980141-G-T

136050317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: synonymous variant
orthologous variants: 25980230-G-A

136050317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: missense variant
orthologous variants: 25980230-G-T

136050655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25980568-C-G

136050719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25980605-G-A

136051439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25981427-C-T

136051459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25981444-C-T

136051510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25981508-C-T

http://identifiers.org/hco/9/GRCh38#136052436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25982426-C-A

136052445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 25982435-G-A

136052445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 25982435-G-T

136052490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 25982476-G-A

136052672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 25982678-G-A

http://identifiers.org/hco/9/GRCh38#136052690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#25982696-A-C

136052725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25982709-G-A

136052833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 25982801-T-G

136053191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25983087-C-T

136053313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25983192-T-C

136053313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25983192-T-G

136053716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25983667-G-A

136054332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25984105-C-T

136054565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25984341-A-G

136054623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25984391-G-A

136055522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25985206-C-T

136056009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25985590-G-A

136056009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25985590-G-C

136056105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25985698-C-T

136056475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25986086-T-C

136056577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25986204-A-G

136056659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25986291-G-A

136056659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25986291-G-T

136056665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25986297-T-C

136056824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25986402-G-A

136057662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25987903-A-G

136057746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25987967-G-A

136057746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25987967-G-T

136057783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25987998-G-A

136057858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25988086-C-G

136057936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25988155-G-A

136057936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25988155-G-C

136057943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25988162-C-G

136057943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25988162-C-T

136058142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25988347-T-C

136059345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25989162-G-A

136059934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25989562-G-A

http://identifiers.org/hco/9/GRCh38#136078164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25996051-C-A

136078214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25996101-C-G

136078347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25996202-A-G

136078347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25996202-A-T

http://identifiers.org/hco/9/GRCh38#136078803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25997948-C-A

136078927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25998051-C-T

136078978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25998100-C-T

136079081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25998199-A-T

136079194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25998303-T-C

136079341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25998466-G-A

136079360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25998483-G-T

136079580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25998726-G-A

136081092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25999736-C-T

136081155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25999807-G-A

136081174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25999826-G-A

136081174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25999826-G-T

136081229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 25999869-C-T

http://identifiers.org/hco/9/GRCh38#136081327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#25999955-C-A

136081973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26000377-G-A

http://identifiers.org/hco/9/GRCh38#136082158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26000475-C-A

136082237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26000523-T-C

136082237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26000523-T-G

136082617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26000740-T-C

136082822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26000934-G-A

136082914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26001028-T-C

136082975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26001084-C-G

136082975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26001084-C-T

136084177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26002778-C-T

136085861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26004384-G-A

136086141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26004591-T-C

136086318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26004756-G-A

136086869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26005544-C-T

http://identifiers.org/hco/9/GRCh38#136087706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26005904-C-A

136087706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26005904-C-T

136087885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26006073-T-C

136088079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26006249-G-A

136088204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26006361-G-A

136088208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26006365-C-T

136088754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26006845-C-G

136088754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26006845-C-T

136088987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26007045-C-T

136089601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26007569-C-G

136089604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26007572-G-A

136089658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 26007625-T-C

136089658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 26007625-T-G

136089785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26007737-T-G

136090049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26008015-C-T

http://identifiers.org/hco/9/GRCh38#136090214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26008139-C-A

http://identifiers.org/hco/9/GRCh38#136090454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26008301-C-A

136090529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26008360-G-A

136090581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26008373-T-G

http://identifiers.org/hco/9/GRCh38#136090792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26008581-C-A

136091003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26008768-G-C

136091199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26008941-G-A

136091229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26008970-G-A

136091229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26008970-G-C

136091644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26009207-G-A

136092009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26009471-G-A

136092066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26009522-C-T

136092072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26009528-G-T

136092549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26010097-G-C

http://identifiers.org/hco/9/GRCh38#136093094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26010658-C-A

136093393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26010956-A-G

136093393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26010956-A-T

http://identifiers.org/hco/9/GRCh38#136094059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26011632-C-A

136094265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 26011830-G-C

136094269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26011834-G-A

136094372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron variant
orthologous variants: 26011946-G-A

136095059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23846
most severe consequence: intron_variant, undefined
orthologous variants: 26012581-G-A