48684904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32907430-G-A

48684904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32907430-G-T

48684961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5 prime UTR variant
orthologous variants: 32907367-T-A

48684961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5 prime UTR variant
orthologous variants: 32907367-T-C

48684986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32907342-A-G

http://identifiers.org/hco/10/GRCh38#48684987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32907341-C-A

48684987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32907341-C-T

48685013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32907316-T-A

http://identifiers.org/hco/10/GRCh38#48685114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32907225-A-C

48685114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, undefined
orthologous variants: 32907225-A-G

48685137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32907200-G-A

48685137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32907200-G-T

48685151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32907189-G-T

48685259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32907101-T-C

48685370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32906981-C-T

48685485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32906887-A-G

48685514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32906858-A-G

48685596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32906759-G-A

http://identifiers.org/hco/10/GRCh38#48685876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32906536-C-A

48685876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32906536-C-T

48685879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32906533-T-C

48685879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32906533-T-G

http://identifiers.org/hco/10/GRCh38#48685881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32906531-C-A

48686049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32906372-C-T

48688395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32902262-T-A

48688395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32902262-T-C

48688793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32901898-T-C

48688848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32901846-G-A

48688848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32901846-G-C

http://identifiers.org/hco/10/GRCh38#48688980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32901733-C-A

48689257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32901461-T-C

48689601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900801-T-A

48689601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900801-T-C

48689608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900794-G-T

48689621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900780-G-A

48689664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900746-G-A

48689664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900746-G-T

48689783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900655-T-A

48689783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900655-T-G

48689799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900642-T-C

48689799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900642-T-G

48689932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32900422-G-A

http://identifiers.org/hco/10/GRCh38#48690089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32900185-C-A

48690365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32899903-T-C

48693191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32896972-A-G

48693670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32896497-A-T

48693800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32896400-T-A

48694044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32896113-G-T

48694096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32896061-T-C

http://identifiers.org/hco/10/GRCh38#48694814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32895019-C-A

http://identifiers.org/hco/10/GRCh38#48694939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32894891-C-A

48695084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32894790-G-A

48695117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32894758-G-T

48695385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32894608-A-T

48695584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32894371-A-T

48695796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32894221-T-C

48695854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32894164-C-T

http://identifiers.org/hco/10/GRCh38#48696147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32893875-C-A

48696147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32893875-C-T

48696190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32893834-G-A

48696205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32893819-C-T

http://identifiers.org/hco/10/GRCh38#48696300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32893709-C-A

48696345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32893671-T-C

48696494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32893530-G-C

48696573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32893448-A-T

48705419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32891081-G-A

48705433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32891067-C-T

48705778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890731-G-A

48705787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890704-G-A

48705837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890633-T-G

48705862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890585-C-T

http://identifiers.org/hco/10/GRCh38#48705896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32890544-A-C

48705967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890417-A-G

48705977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890397-G-A

48706158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890229-G-T

48706276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32890101-C-T

48706499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32889910-G-A

48706499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32889910-G-C

48706524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32889886-T-C

48706573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32889826-C-T

48707061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32888266-C-G

48707061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32888266-C-T

48707216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32888141-A-G

48707288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32888076-A-G

48707326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32888043-G-A

48707332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32888037-T-C

http://identifiers.org/hco/10/GRCh38#48707352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32888017-C-A

48708609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32886335-T-A

48708620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32886324-C-T

http://identifiers.org/hco/10/GRCh38#48709494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32885132-C-A

48709552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32885071-A-G

48709639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32884993-A-G

http://identifiers.org/hco/10/GRCh38#48709658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32884974-C-A

http://identifiers.org/hco/10/GRCh38#48709664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32884970-C-A

48709796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32884835-G-T

48709810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32884821-T-C

48709874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32884757-G-A

48713028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32884081-A-T

48713057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32884052-G-A

48713116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32883996-G-C

48713179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32883936-A-G

48713616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32883786-C-T

48713756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32883645-C-T

48713765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32883636-T-C

48713794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32883618-C-G

48714256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32882469-T-C

48714572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32882168-G-A

48714572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32882168-G-C

http://identifiers.org/hco/10/GRCh38#48714817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32881930-C-A

48715580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32880741-A-G

48716441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32880215-T-C

48719892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32877837-G-A

48720119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32877618-C-T

http://identifiers.org/hco/10/GRCh38#48720147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32877561-C-A

48720147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32877561-C-T

48720345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32877179-C-G

48720491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876887-A-G

48720825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876476-A-G

48721096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876221-G-A

48721194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876127-G-A

48721194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876127-G-T

48721199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876122-G-A

48721244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876093-G-A

48721244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32876093-G-T

48721272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32876060-T-C

48721307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32876025-C-T

48721308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32876024-G-A

48721308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32876024-G-T

48721442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32875891-T-G

48721482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32875866-T-C

http://identifiers.org/hco/10/GRCh38#48721509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32875841-C-A

48721509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32875841-C-G

48721509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32875841-C-T

48721644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32875573-C-T

48722313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32874920-T-C

http://identifiers.org/hco/10/GRCh38#48723300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32874754-C-A

48723300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32874754-C-T

48723349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32874696-G-A

48723349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32874696-G-T

48723357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32874695-G-A

48723357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32874695-G-T

48723523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32874538-G-A

http://identifiers.org/hco/10/GRCh38#48723704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32874382-C-A

48723704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32874382-C-T

48725727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873862-C-G

48725727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873862-C-T

48725737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873852-T-C

48725773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873814-T-A

48725773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873814-T-C

48725902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32873693-G-T

48725911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32873684-G-C

48725911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32873684-G-T

48726066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32873529-G-A

48726066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32873529-G-T

http://identifiers.org/hco/10/GRCh38#48726104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32873491-C-A

48726104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873491-C-T

http://identifiers.org/hco/10/GRCh38#48726120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32873475-C-A

48726121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873474-T-C

48726126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873470-C-T

http://identifiers.org/hco/10/GRCh38#48726183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32873434-C-A

48726183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873434-C-T

48726234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873390-G-A

48726286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873338-C-T

48726594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873097-T-C

48726650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32873057-G-A

http://identifiers.org/hco/10/GRCh38#48726802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32872306-A-C

http://identifiers.org/hco/10/GRCh38#48726879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32872272-C-A

48727077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32872008-A-G

48727125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871962-A-G

http://identifiers.org/hco/10/GRCh38#48727377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32871725-C-A

48727377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871725-C-T

48727398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871692-G-T

48727401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871689-A-G

48727401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871689-A-T

48727411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871679-T-C

48727418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871672-A-G

48727433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871659-A-G

48727439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871653-A-G

48727529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32871567-G-A

48727668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871428-C-T

48727682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871414-G-A

48727694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871399-G-A

http://identifiers.org/hco/10/GRCh38#48727769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32871287-C-A

48727769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871287-C-T

48727879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871160-G-A

48727906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871129-G-A

48727933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32871112-G-A

48728194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870852-C-T

48728204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870843-C-T

48728261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870789-T-C

48728359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870709-C-T

48728670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870433-G-A

48728724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870372-G-T

48728737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870359-T-G

48728738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870358-G-A

48728959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32870165-G-A

48729090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869986-G-A

48729104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869976-T-C

48729124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869956-G-A

48729359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869117-T-C

48729363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869111-G-A

48729363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869111-G-C

48729375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869099-C-T

48729397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869077-G-A

48729397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32869077-G-C

http://identifiers.org/hco/10/GRCh38#48729410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32869074-C-A

48729460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32869025-G-T

http://identifiers.org/hco/10/GRCh38#48729481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32869004-C-A

48729505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32868980-A-G

http://identifiers.org/hco/10/GRCh38#48729683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32868806-C-A

48729683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32868806-C-T

48729704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32868794-T-A

48730011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32868418-A-G

48730062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32868371-C-T

48730119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32868332-C-G

48730271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32868175-C-T

48730491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867966-G-C

48730525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867945-G-T

48730844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867640-T-C

48730926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867544-C-T

48730973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867483-A-G

48730973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867483-A-T

http://identifiers.org/hco/10/GRCh38#48730985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32867473-C-A

48731028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867430-G-A

48731028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867430-G-C

48731028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867430-G-T

48731094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32867366-T-A

http://identifiers.org/hco/10/GRCh38#48731151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32867308-A-C

48731302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32867157-C-T

48731364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 32867095-G-A

48731364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 32867095-G-C

48731415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant
orthologous variants: 32867044-G-A

48731430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant
orthologous variants: 32867029-C-T

48731607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866852-G-A

48731607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866852-G-T

http://identifiers.org/hco/10/GRCh38#48731638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32866829-C-A

48731638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866829-C-T

http://identifiers.org/hco/10/GRCh38#48731643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32866824-C-A

48731643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866824-C-G

48731643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866824-C-T

48731693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866764-G-A

48731693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866764-G-T

48731710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866747-A-G

48732243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866409-G-A

48732451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866198-G-A

48732526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32866121-A-T

48732627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32865994-C-T

48732703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32865929-G-T

48732765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32865874-G-A

48732768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32865871-G-A

48732783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32865856-T-C

http://identifiers.org/hco/10/GRCh38#48733137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32865144-A-C

48733137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32865144-A-G

48733248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32865033-G-A

48733331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864948-T-C

48733424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864855-G-A

48733484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864800-A-G

48733769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864553-T-A

48733780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864542-G-A

48733780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864542-G-T

48733804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864518-A-G

48733893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864425-A-G

48734003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32864315-T-C

48734043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32864275-T-A

48734053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864265-T-C

http://identifiers.org/hco/10/GRCh38#48734084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32864235-C-A

http://identifiers.org/hco/10/GRCh38#48734125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32864222-C-A

http://identifiers.org/hco/10/GRCh38#48734140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32864207-A-C

48734140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864207-A-G

http://identifiers.org/hco/10/GRCh38#48734143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32864205-C-A

48734143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864205-C-T

http://identifiers.org/hco/10/GRCh38#48734146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32864202-C-A

48734146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864202-C-T

48734151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864201-G-A

48734212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32864152-T-C

48734599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863889-A-G

48734599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863889-A-T

48734624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863862-T-A

48734624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863862-T-C

48734647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863836-A-G

48734719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863778-T-G

48734824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863685-G-T

48735348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863242-A-T

48735526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32863035-C-T

http://identifiers.org/hco/10/GRCh38#48735646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32862908-C-A

48735751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862802-G-A

48735774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862784-G-T

48735839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862722-T-C

http://identifiers.org/hco/10/GRCh38#48735840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32862721-C-A

48735840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862721-C-T

48735871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862690-G-T

48735945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32862616-G-A

http://identifiers.org/hco/10/GRCh38#48736191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32862389-C-A

48736191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32862389-C-T

48736200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32862380-G-T

48736282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862126-G-A

48736282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862126-G-C

48736282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32862126-G-T

http://identifiers.org/hco/10/GRCh38#48736346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32862063-C-A

48736493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32861918-G-A

48736864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32861549-G-C

48737528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32860742-T-G

48737808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32860435-T-C

48738221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32860081-A-G

48738247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32860055-T-C

48738507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32859799-G-A

48738866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32859409-C-T

48738960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32859340-C-T

48739422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32858880-C-T

48739766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32858539-G-A

48739852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32858464-T-C

48740087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32858243-T-C

48740265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32858053-T-A

http://identifiers.org/hco/10/GRCh38#48741658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32857674-C-A

48741668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32857664-A-G

48741678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32857654-C-T

48741683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32857648-C-T

http://identifiers.org/hco/10/GRCh38#48741829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32857515-A-C

48741862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32857490-G-A

48742136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32857247-C-T

48742166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32857217-A-T

48742358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32856903-A-G

48742475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32856795-A-G

48742489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32856781-C-T

48743081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32855619-C-T

48743148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855552-G-A

48743157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855543-G-A

48743157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855543-G-C

48743157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855543-G-T

48743271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855429-G-A

48743432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32855268-T-C

48743432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32855268-T-G

48743467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855233-G-A

48743467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855233-G-T

48743502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32855201-A-G

http://identifiers.org/hco/10/GRCh38#48743553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32855138-C-A

48743553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32855138-C-T

48744306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32854455-C-T

48744309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32854452-C-T

48744335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32854424-C-T

48744369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32854409-A-G

http://identifiers.org/hco/10/GRCh38#48744678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32854067-A-C

48744695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32854050-T-A

48744980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32853416-A-G

48745030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32853363-T-C

48745044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32853336-G-C

48745122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32853245-T-C

48745122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32853245-T-G

48745216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32853161-T-C

48745413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32852963-T-G

48745461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32852926-T-C

48760213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32847989-T-C

48760415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32847824-G-A

48760415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32847824-G-T

48762265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32847623-C-T

48762783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846947-A-G

http://identifiers.org/hco/10/GRCh38#48762795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32846935-C-A

48762795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846935-C-T

http://identifiers.org/hco/10/GRCh38#48763044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32846666-C-A

48763044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846666-C-T

48763124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846585-A-G

http://identifiers.org/hco/10/GRCh38#48763311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32846429-C-A

48763311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846429-C-G

http://identifiers.org/hco/10/GRCh38#48763339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32846387-A-C

48763445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846296-C-T

48763447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846293-C-G

48763668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32846083-T-A

48764235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32845544-C-T

48764278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32845522-C-G

48764397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32845399-T-C

48764548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32845265-C-T

48764623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32845210-A-T

48765114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32844802-T-C

48765155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32844767-G-A

48765189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32844734-A-G

48765190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32844733-A-T

48765211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32844712-T-C

48765361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32844590-T-C

48765922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32840296-C-G

48765922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32840296-C-T

48766056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32840158-G-A

48766101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32840114-A-G

48766116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32840099-G-A

48766150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32840070-C-T

48766630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839952-C-T

48766707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839877-C-T

48766825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839793-G-A

48766825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839793-G-T

48766843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839775-C-T

48766871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839749-G-A

48766942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839682-C-T

48766969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839655-A-G

48767109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839526-C-T

48767110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839525-A-G

48767278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839388-C-T

48767695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839138-A-G

48767695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32839138-A-T

48767844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32838993-G-C

48768198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32838488-G-A

http://identifiers.org/hco/10/GRCh38#48768378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32838305-C-A

48768409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32838271-C-G

48768798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837722-A-G

48768843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837679-A-G

48768843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837679-A-T

48768844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837678-C-T

48768856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837667-C-G

48768877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837647-C-G

48768877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837647-C-T

48768932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32837591-G-A

48769344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32836671-A-G

48769587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32836433-G-A

48769784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, undefined
orthologous variants: 32835824-G-A

48769792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, undefined
orthologous variants: 32835816-T-A

48770458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32835148-G-C

48770531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32835076-T-A

48770644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32834971-C-T

48770667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32834948-G-A

48770819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32834791-C-T

48771303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32833561-C-G

48771333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32833539-T-G

http://identifiers.org/hco/10/GRCh38#48771335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32833537-C-A

http://identifiers.org/hco/10/GRCh38#48771643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32833258-A-C

48771643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32833258-A-G

48771726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32833181-G-A

48772364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32832627-T-C

48772402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32832593-C-T

48773829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32832221-G-A

48774036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32832022-G-A

48774312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831778-G-T

48774340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831757-T-G

48774395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831736-A-G

48774403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831728-T-A

http://identifiers.org/hco/10/GRCh38#48774418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32831713-C-A

48774421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831710-C-T

48774451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32831679-C-T

48774494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32831636-A-G

48774536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32831594-T-C

48774566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32831564-G-A

http://identifiers.org/hco/10/GRCh38#48774693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32831435-A-C

48774749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831392-A-G

48774757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831386-G-T

48774770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831373-G-T

http://identifiers.org/hco/10/GRCh38#48774873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32831307-C-A

48774898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831284-G-C

48774928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831258-T-C

48775188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831108-G-A

48775227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831081-G-A

48775297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32831028-G-A

http://identifiers.org/hco/10/GRCh38#48775325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32830998-C-A

48775337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830986-G-T

48775559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830794-C-T

48775568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830787-T-C

48775568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830787-T-G

48775637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830729-G-A

48775637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830729-G-C

48775637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830729-G-T

http://identifiers.org/hco/10/GRCh38#48775643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32830723-A-C

48775643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830723-A-T

48775739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32830636-A-G

48775752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32830623-A-G

http://identifiers.org/hco/10/GRCh38#48775753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32830622-C-A

48775753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32830622-C-G

http://identifiers.org/hco/10/GRCh38#48775838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32830543-A-C

48775838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830543-A-G

48775904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830471-G-T

48776061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830361-G-A

48776345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830093-G-A

48776377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830083-C-T

48776409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32830058-C-T

48776480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32829993-A-G

http://identifiers.org/hco/10/GRCh38#48776704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32829837-A-C

http://identifiers.org/hco/10/GRCh38#48776708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32829833-C-A

48776708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32829833-C-T

48776775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32829773-T-C

http://identifiers.org/hco/10/GRCh38#48776920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32829640-C-A

48776920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: stop gained
orthologous variants: 32829640-C-T

48776941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32829619-G-A

48776941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32829619-G-T

http://identifiers.org/hco/10/GRCh38#48777061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32829499-C-A

48777192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32829357-G-T

48777291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32829256-T-G

http://identifiers.org/hco/10/GRCh38#48777371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32829183-A-C

48777371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32829183-A-G

48777429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32829125-A-G

48777593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32829000-A-T

http://identifiers.org/hco/10/GRCh38#48777626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32828982-C-A

48777626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828982-C-T

48777851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828905-T-A

48778306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828498-A-T

48778307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828497-G-C

48778471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828337-A-G

48778479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828329-G-A

48778480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828328-A-G

http://identifiers.org/hco/10/GRCh38#48778516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32828292-C-A

48778516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828292-C-T

48778564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828220-C-T

48778570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828206-G-T

48778582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32828194-C-T

48778649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32828126-T-C

48778872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827898-G-A

48778872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827898-G-C

48778872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827898-G-T

48778921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827854-A-G

48779017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827756-G-T

48779111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827696-C-T

48779114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827693-T-C

48779284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827463-A-G

48779305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32827430-G-A

48779608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826969-C-T

48779639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826930-G-A

48779693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826803-G-A

48779787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826691-A-G

48779829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826643-G-A

48779842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826628-A-G

48779866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826602-T-C

http://identifiers.org/hco/10/GRCh38#48779881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32826586-C-A

48779881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826586-C-T

48779892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826575-C-T

48779898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826569-T-A

48779898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826569-T-C

http://identifiers.org/hco/10/GRCh38#48779903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32826564-C-A

48779942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 32826525-T-A

48786562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32826168-A-G

48786765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32825966-G-A

48786825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32825906-C-T

48787000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32825733-T-C

48787458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32825283-C-T

48787665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32825072-G-T

48787883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824964-T-C

48788161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824864-G-C

48788552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: synonymous variant
orthologous variants: 32824606-C-T

48788562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32824596-G-A

48788659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32824499-G-A

48788716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824435-G-A

48788716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824435-G-T

48788800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824354-G-A

48788800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824354-G-C

48788800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824354-G-T

48788889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824273-A-G

48788983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32824180-A-T

48789503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823892-G-C

48789505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823890-G-A

48789639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823789-G-A

48789639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823789-G-C

48789700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823729-T-A

http://identifiers.org/hco/10/GRCh38#48789737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32823704-C-A

48789737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823704-C-G

48789737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823704-C-T

48789999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823445-G-C

48790006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823438-T-A

48790101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823357-G-T

48790118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823341-T-A

48790118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823341-T-C

48790118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823341-T-G

48790127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823332-A-G

48790132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823327-A-G

http://identifiers.org/hco/10/GRCh38#48790658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32823106-C-A

48790658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823106-C-T

48790697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32823080-T-C

http://identifiers.org/hco/10/GRCh38#48790814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32822963-C-A

48790814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32822963-C-G

48790814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32822963-C-T

48790858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32822919-T-A

48790858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32822919-T-C

48790933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822844-C-T

http://identifiers.org/hco/10/GRCh38#48790960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32822817-C-A

48790960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822817-C-G

48790960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822817-C-T

48791343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822393-T-C

48791471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822252-A-G

48791481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822242-T-C

48791522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822207-G-A

48791574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822150-C-T

48791577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822147-A-G

48791597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32822128-A-G

48795563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821947-T-C

48795603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821907-C-T

http://identifiers.org/hco/10/GRCh38#48795765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32821738-C-A

48795765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821738-C-T

http://identifiers.org/hco/10/GRCh38#48795806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32821697-A-C

48795966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821539-A-G

48795985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821515-G-T

48796149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821403-T-C

48796149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821403-T-G

48796191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821361-T-C

48796193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821359-G-A

48796193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821359-G-T

48796242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32821186-G-T

48796382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32821040-G-A

48796393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32821029-C-G

48796482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32820940-G-A

48796482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32820940-G-T

48796484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32820938-G-A

48796484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32820938-G-C

48796484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32820938-G-T

48796488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32820934-G-A

http://identifiers.org/hco/10/GRCh38#48796580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32820842-A-C

48803319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32819778-A-G

48803383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819715-G-A

48803397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819701-A-G

48803414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819684-C-T

48803464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819627-G-T

48803514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819587-G-A

48803636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819418-C-G

48803794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819277-G-A

48803898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819202-C-T

48803923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819184-C-T

48803926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819181-G-A

http://identifiers.org/hco/10/GRCh38#48803965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32819141-C-A

48804061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32819035-C-T

48804522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32818737-A-G

48804588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32818686-T-A

48804588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32818686-T-G

48804713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32818596-T-C

http://identifiers.org/hco/10/GRCh38#48804901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32818407-C-A

48804901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32818407-C-T

48805220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32818088-C-G

48805351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32817957-A-G

48805450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817851-A-G

http://identifiers.org/hco/10/GRCh38#48805490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32817811-C-A

48805490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817811-C-T

http://identifiers.org/hco/10/GRCh38#48805502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32817799-C-A

48805539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817767-G-A

48805539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817767-G-T

48805543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817763-T-A

48805543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817763-T-G

48805557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817749-G-C

48805557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817749-G-T

48805562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817744-T-A

48805562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817744-T-C

48805562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817744-T-G

48805566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817740-G-A

48805566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817740-G-C

48805641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817683-T-C

48805797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817529-T-C

48805869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817458-G-T

48805877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817450-T-G

48805897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817422-T-C

48805913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817406-G-A

48805913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817406-G-C

48805913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817406-G-T

48805943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817375-G-A

48805943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817375-G-T

48806005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32817314-A-G

48806059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32817260-A-G

http://identifiers.org/hco/10/GRCh38#48806092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32817227-C-A

http://identifiers.org/hco/10/GRCh38#48806201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32817105-C-A

48806201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817105-C-G

48806201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32817105-C-T

48806387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32816946-T-C

48806387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32816946-T-G

48806503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32816843-T-C

48806872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32816182-T-C

http://identifiers.org/hco/10/GRCh38#48806875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32816179-A-C

http://identifiers.org/hco/10/GRCh38#48806916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32816138-A-C

48806942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32816112-C-T

48807122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815939-A-G

48807228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815858-G-C

48807274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815818-T-A

48807274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815818-T-G

48807392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815752-A-G

48807486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815701-T-G

http://identifiers.org/hco/10/GRCh38#48807714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32815445-C-A

48807763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815396-G-T

http://identifiers.org/hco/10/GRCh38#48807804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32815361-A-C

http://identifiers.org/hco/10/GRCh38#48807825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32815340-C-A

48807825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815340-C-T

48808109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32815045-T-C

48808153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32814999-G-T

48808293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32814860-T-C

48808603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814560-C-T

48809602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813760-T-C

48809654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813709-A-G

48809689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813672-C-T

48809698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813663-C-G

48809890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813465-C-T

48809903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813452-C-T

48809914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813441-G-A

48809917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813438-C-T

48810095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813318-C-T

48810192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813248-A-G

48810232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813227-T-C

48810328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813139-A-G

http://identifiers.org/hco/10/GRCh38#48810353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32813114-A-C

48810353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813114-A-G

48810392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813078-A-G

48810392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813078-A-T

48810447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813032-G-A

48810447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813032-G-C

48810455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813024-G-T

48810506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812977-T-C

48810612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32812870-G-T

48810613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32812869-T-G

48810672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32812810-A-G

http://identifiers.org/hco/10/GRCh38#48810704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32812778-A-C

48810885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812647-G-A

48810885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812647-G-T

48811099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812427-C-T

48811531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32811985-A-G

http://identifiers.org/hco/10/GRCh38#48811718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32811798-C-A

48811815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811705-G-A

48811815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811705-G-C

48811815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811705-G-T

http://identifiers.org/hco/10/GRCh38#48811833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32811688-C-A

48811833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811688-C-T

http://identifiers.org/hco/10/GRCh38#48811855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32811666-C-A

48811855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811666-C-T

48812140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811432-G-A

48812144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811428-C-G

48812155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811420-A-T

48812543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811246-A-G

http://identifiers.org/hco/10/GRCh38#48812762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32811168-C-A

48812887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811022-T-C

48812892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811017-T-G

48813053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810923-G-A

48813053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810923-G-C

48813174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810807-A-G

48813251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810747-T-C

48813274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810719-T-C

48813279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810714-A-G

48813464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810536-G-A

48813691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810328-G-T

48813693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810326-A-G

48813739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810222-T-A

48813739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810222-T-G

http://identifiers.org/hco/10/GRCh38#48813847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32810125-C-A

48813847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810125-C-T

http://identifiers.org/hco/10/GRCh38#48813876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32810096-A-C

48813876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810096-A-G

48813876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810096-A-T

48813882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810089-G-T

48813899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810073-G-A

48813899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810073-G-T

http://identifiers.org/hco/10/GRCh38#48813935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32810046-C-A

48813935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810046-C-G

48813935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32810046-C-T

http://identifiers.org/hco/10/GRCh38#48813999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32809982-C-A

48814044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32809937-T-G

http://identifiers.org/hco/10/GRCh38#48814077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32809904-A-C

48814077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32809904-A-G

48814102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809879-T-C

48814161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809823-T-C

48814677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809298-C-T

48814802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809177-C-T

http://identifiers.org/hco/10/GRCh38#48814862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32809112-C-A

48814862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809112-C-T

48814899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809075-C-T

http://identifiers.org/hco/10/GRCh38#48814959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32809012-A-C

48814959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809012-A-G

48814959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809012-A-T

48815019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808937-A-G

48815084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808868-G-A

48815092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808860-G-A

48815150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808803-A-G

48815219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808708-C-T

http://identifiers.org/hco/10/GRCh38#48815251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32808676-C-A

48815251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808676-C-G

48815256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808671-G-A

48815274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808656-T-C

48815274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808656-T-G

48815305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808636-A-G

48815965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32807891-T-C

48815972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32807884-G-A

48815972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32807884-G-T

http://identifiers.org/hco/10/GRCh38#48816697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32807121-A-C

48816766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32807049-T-A

48816931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32806935-C-T

48817053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805968-C-T

http://identifiers.org/hco/10/GRCh38#48817094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32805939-C-A

48817094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805939-C-T

48817119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805914-G-T

48817193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805830-A-G

48817210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805815-C-T

48817219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805786-A-G

48817220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805785-C-T

48817221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805784-T-C

48817222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805783-A-G

http://identifiers.org/hco/10/GRCh38#48817264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32805740-A-C

48817266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32805738-G-A

48817267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32805737-G-A

48817292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32805712-C-T

http://identifiers.org/hco/10/GRCh38#48817310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32805694-C-A

48817322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32805682-C-T

48817371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32805633-A-T

48817477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805524-G-A

48817477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805524-G-T

http://identifiers.org/hco/10/GRCh38#48817512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32805490-C-A

48817512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805490-C-T

48817698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805285-G-A

48817952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805030-T-C

48818170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804835-G-A

48818236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804779-G-A

48818310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804726-G-A

48818348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804689-A-G

48818841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32803915-C-T

48818880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32803886-A-G

48818949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32803822-G-T

48819209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32803558-G-C

48819850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802990-C-T

48820107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802873-G-A

48820107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802873-G-T

http://identifiers.org/hco/10/GRCh38#48820122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32802860-C-A

48820260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32802731-C-T

48820365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32802626-G-T

48820411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32802580-T-A

48820411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32802580-T-C

48820411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32802580-T-G

48820438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 32802553-G-A

48820456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802533-C-T

48820530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802471-G-A

48820530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802471-G-T

48820821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802189-A-G

http://identifiers.org/hco/10/GRCh38#48820951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32802054-C-A

48821022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802006-G-A

48821022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802006-G-T

http://identifiers.org/hco/10/GRCh38#48821024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32802004-C-A

48821024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802004-C-T

48821049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801979-G-A

48821049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801979-G-C

48821049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801979-G-T

48821113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32801915-G-A

48821155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32801873-G-A

48821164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32801864-G-A

48821164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32801864-G-T

48821205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801815-T-G

http://identifiers.org/hco/10/GRCh38#48821225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32801787-C-A

48821225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801787-C-G

48821225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801787-C-T

http://identifiers.org/hco/10/GRCh38#48821237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32801775-A-C

http://identifiers.org/hco/10/GRCh38#48821239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32801773-C-A

48821269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801751-T-A

48821269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801751-T-C

http://identifiers.org/hco/10/GRCh38#48821286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32801734-A-C

48821286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801734-A-G

48821388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801641-T-A

48821388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801641-T-C

48821415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801614-C-T

48821419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801610-T-C

48821424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801604-C-G

48821605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801427-C-T

48821711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801340-T-C

48821734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801318-A-T

48821744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801308-G-C

48821953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801102-T-C

48822164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800511-C-G

48822164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800511-C-T

http://identifiers.org/hco/10/GRCh38#48822265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32800429-C-A

48822283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800413-T-G

48822353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800348-A-G

48822369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800332-T-C

48822382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32800317-G-A

48822401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32800298-G-A

48822401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32800298-G-T

http://identifiers.org/hco/10/GRCh38#48822467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32800232-A-C

48822467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32800232-A-G

48822534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32800165-G-T

48822587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800125-T-C

48822614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800100-T-A

48822614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800100-T-C

http://identifiers.org/hco/10/GRCh38#48822631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32800080-C-A

48822631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800080-C-G

48822631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800080-C-T

http://identifiers.org/hco/10/GRCh38#48822650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32800055-C-A

48822650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800055-C-G

48822653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800052-G-C

48822653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800052-G-T

48823941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32799831-A-T

48824053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32799735-G-A

48824053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32799735-G-T

48824065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32799723-T-A

http://identifiers.org/hco/10/GRCh38#48824120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32799678-C-A

48824174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32799622-G-T

http://identifiers.org/hco/10/GRCh38#48824191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32799603-C-A

48824191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32799603-C-T

48824205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32799589-C-G

48824251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32799545-T-C

48824282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32799514-A-G

48824658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32799091-A-G

http://identifiers.org/hco/10/GRCh38#48826608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32798500-C-A

48826608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32798500-C-T

48826681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32798431-C-T

48826866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32798246-C-T

48827042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32798082-T-G

48827256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32797879-T-C

48827406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32797728-T-G

48828092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32796200-T-C

48828098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32796194-T-C

48828857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32795459-G-A

48828857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32795459-G-T

48828890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32795423-A-G

48830344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32793019-G-T

48830497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792869-T-G

http://identifiers.org/hco/10/GRCh38#48830590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32792797-C-A

48830590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792797-C-T

48830641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792770-G-C

48830678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792742-T-C

48830726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: stop gained
orthologous variants: 32792694-C-T

48830729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32792691-A-T

48830888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792532-C-T

http://identifiers.org/hco/10/GRCh38#48830927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32792493-C-A

48830927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792493-C-G

48830927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792493-C-T

48830963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792457-G-T

http://identifiers.org/hco/10/GRCh38#48830964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32792456-C-A

48830974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792447-T-C

48831010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792391-A-G

48831010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792391-A-T

48831012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792389-G-T

http://identifiers.org/hco/10/GRCh38#48831106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32792296-A-C

48831390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32792059-A-G

48831460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32791992-C-T

48831830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791646-T-C

48831865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791611-A-G

48832234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791275-G-A

48832344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791142-T-C

48832358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791131-T-C

http://identifiers.org/hco/10/GRCh38#48832478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32791013-C-A

48832478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791013-C-T

48832491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791000-G-A

48832491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791000-G-C

48832491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32791000-G-T

48832492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790999-G-A

48832492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790999-G-T

48832497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790994-T-G

48832547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790936-G-A

48832547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790936-G-T

48832575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32790913-T-C

48832780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790712-C-T

http://identifiers.org/hco/10/GRCh38#48832806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32790689-C-A

48832826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790670-G-A

48832826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790670-G-T

http://identifiers.org/hco/10/GRCh38#48832827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32790669-C-A

48832827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790669-C-T

http://identifiers.org/hco/10/GRCh38#48832853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32790643-C-A

48832853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32790643-C-T

http://identifiers.org/hco/10/GRCh38#48836614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32789784-A-C

48836650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32789748-C-G

48836684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32789674-T-C

48836969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32789380-T-C

48837037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32789172-A-G

48837121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32789009-G-C

48837251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788874-G-C

48837346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788793-G-A

48837360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788783-C-G

48837363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788780-G-A

48837363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788780-G-T

48837453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788689-C-T

48837523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788635-C-G

48837545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788603-G-A

48837697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788460-T-G

48837802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788366-A-G

48837802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788366-A-T

48837861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788299-C-T

48837905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788258-A-G

48837920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32788244-T-C

http://identifiers.org/hco/10/GRCh38#48838271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32787972-A-C

48838271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787972-A-G

48838551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787736-A-T

48838750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787603-C-T

48838897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787484-G-T

48838937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787443-G-A

48839205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787228-G-C

48839308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787119-T-G

48839338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787088-A-G

48839418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787012-G-A

http://identifiers.org/hco/10/GRCh38#48839453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32786977-A-C

48839602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786829-T-G

48840774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785338-T-C

48840845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785261-C-T

48841392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784746-A-T

48841454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784688-T-A

48841681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784315-C-T

48841813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784179-A-T

48841817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784175-T-C

48841817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784175-T-G

48841855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784134-A-G

48841865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784124-G-A

48842263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32783763-A-G

48842364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32783659-A-G

48842370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32783653-T-C

http://identifiers.org/hco/10/GRCh38#48842549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32783446-C-A

48842819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32783208-C-T

48842912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32783140-C-G

48843077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32783000-T-C

48843108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782969-A-T

48843606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782940-A-G

48843609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782937-G-T

48843845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782731-G-A

48843845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782731-G-C

48843845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782731-G-T

48843846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782730-T-C

48844198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782366-G-A

48844794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782069-G-C

48844803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782060-A-G

48845112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781835-G-A

48845125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781822-G-T

http://identifiers.org/hco/10/GRCh38#48845230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32781724-A-C

48845262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781692-T-G

48845268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781686-T-A

48845268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781686-T-C

48845465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781544-G-A

48845584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781430-G-T

48845778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781251-G-A

48845790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781239-A-T

http://identifiers.org/hco/10/GRCh38#48845853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32781174-C-A

48846035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32780994-A-G

48846187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32780882-A-G

48846749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32780426-G-C

48846782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32780351-G-A

48847924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32779148-C-T

48848064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32779008-C-G

48848233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32778885-T-A

48848234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32778884-A-G

48849845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32778108-G-T

48850108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32777869-G-A

48850195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32777789-A-G

http://identifiers.org/hco/10/GRCh38#48850257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32777727-A-C

48850276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32777706-T-C

48850475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32777506-C-T

http://identifiers.org/hco/10/GRCh38#48850612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32777258-C-A

48850612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32777258-C-T

48850898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32776993-A-G

48851048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32776760-G-A

http://identifiers.org/hco/10/GRCh38#48851172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32776677-C-A

48851267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32776620-C-T

48851714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32776254-T-C

http://identifiers.org/hco/10/GRCh38#48851884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32776107-A-C

48851885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32776106-G-A

http://identifiers.org/hco/10/GRCh38#48851933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32776050-C-A

48851933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32776050-C-G

48852222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775758-G-A

48852222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775758-G-T

48852223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775757-G-C

48852324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775678-G-A

48852383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775617-T-C

48852512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775511-A-T

48852570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775466-C-G

48852669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775366-G-A

48852693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775343-C-T

48852735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775301-T-C

48852749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775287-C-T

48852754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775285-T-A

48852790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775249-C-T

48852861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775147-T-A

48852882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32775128-C-T

48852994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32774966-C-G

48852994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32774966-C-T

48853196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32774485-T-A

48853239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32774448-C-T

48853272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32774415-T-C

48853548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773999-C-T

48853562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773980-A-G

48853669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773868-C-G

48853979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773599-G-A

48854515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773198-G-A

48854515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773198-G-C

48854616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773095-C-T

48854669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32773042-C-T

48854767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772942-T-C

48854876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772841-C-T

48854891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772826-A-G

48854907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772809-A-G

http://identifiers.org/hco/10/GRCh38#48855067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32772644-A-C

http://identifiers.org/hco/10/GRCh38#48855277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32772376-C-A

48855303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772347-C-T

48855318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772333-A-G

48855326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772327-C-T

48855347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772299-T-C

48855431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772216-G-T

48855486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772154-G-A

48855507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32772135-C-T

48855701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32771942-A-G

48866584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32769623-C-T

48867316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32769227-G-A

48867316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32769227-G-T

48867350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32769193-A-G

48867364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32769179-T-A

48867364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32769179-T-C

48867428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32769090-A-G

48867510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32768472-G-A

48867862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32768213-A-G

48867901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32768174-G-C

http://identifiers.org/hco/10/GRCh38#48867976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32768120-C-A

48868118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32767973-G-A

48868118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32767973-G-T

48868455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32767737-G-A

48868455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32767737-G-T

48868541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32767658-T-A

48868582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32767616-T-C

48868583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32767615-T-C

http://identifiers.org/hco/10/GRCh38#48869225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32767000-A-C

48869347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32766535-G-T

48869353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32766529-C-G

http://identifiers.org/hco/10/GRCh38#48869374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32766517-C-A

48869395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32766497-C-G

48869828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32766094-T-G

48870012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32765910-C-T

48872583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32765399-A-G

48872588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32765394-C-T

48872624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32765361-G-A

48872857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32765139-G-C

48872934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32765061-G-A

48873100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32764936-T-C

48873278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32764821-C-T

48873691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense variant
orthologous variants: 32764426-G-T

48873814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32764335-A-G

http://identifiers.org/hco/10/GRCh38#48873970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32764188-C-A

48874057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32764124-T-C

48874199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763975-C-G

48874199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763975-C-T

http://identifiers.org/hco/10/GRCh38#48874220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32763944-A-C

48874343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763817-A-G

48874429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763724-G-A

48874783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763448-G-A

48874814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763418-A-G

http://identifiers.org/hco/10/GRCh38#48875048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32763201-C-A

48875048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763201-C-T

48875189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763054-T-C

48875189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763054-T-G

48875205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32763038-A-G

48875288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32762947-G-A

48875288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32762947-G-T

48875723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32762363-C-G

48875723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32762363-C-T

48875773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32762312-T-C

48875896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32762212-G-C

48875919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32762189-C-T

http://identifiers.org/hco/10/GRCh38#48876099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32762026-C-A

48876234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32761888-G-A

48876288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32761382-G-T

http://identifiers.org/hco/10/GRCh38#48876323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32761347-A-C

48876388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32761286-T-C

48876388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32761286-T-G

48876605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32761084-T-A

48876605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32761084-T-C

48876893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760807-G-A

48876893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760807-G-T

48876960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760752-A-G

http://identifiers.org/hco/10/GRCh38#48877312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32760404-C-A

48877312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760404-C-T

48877350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760377-G-A

48877572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760221-G-A

48877611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760188-T-C

48877698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760119-T-C

48877705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760112-A-G

48877728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760090-T-C

48877730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760088-G-A

48877771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32760047-G-A

http://identifiers.org/hco/10/GRCh38#48879700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32759628-C-A

http://identifiers.org/hco/10/GRCh38#48879893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32759484-A-C

48879893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32759484-A-G

48880251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32759226-C-G

48880580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32758924-C-T

48880683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32758803-G-T

http://identifiers.org/hco/10/GRCh38#48880700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32758786-C-A

48880756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32758731-G-C

http://identifiers.org/hco/10/GRCh38#48883266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32758008-C-A

48883359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32757920-T-C

48883968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32757478-G-C

48883998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32757451-C-T

48884020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32757432-T-C

48884182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32757254-C-T

48884391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32757055-G-T

48884510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32756953-G-A

48884535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32756932-T-A

48884856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32756728-C-G

48885153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32756459-G-T

48885390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32755762-A-G

48885583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32755580-G-A

48886179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32754841-T-A

http://identifiers.org/hco/10/GRCh38#48886254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32754784-C-A

http://identifiers.org/hco/10/GRCh38#48886270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32754768-C-A

48886295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32754743-G-A

48886750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32754679-A-G

48887202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32754224-G-A

48887202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32754224-G-T

48887272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32754156-C-T

48887335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32754097-A-T

48889691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32752424-G-C

48889768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32752351-G-A

48889774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32752345-G-A

48889937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32752230-G-A

48889959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32752224-C-T

48890112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32752109-T-A

http://identifiers.org/hco/10/GRCh38#48890460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32751160-A-C

48890529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32751109-A-G

48890547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32751086-C-T

48890606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32751023-G-A

48890660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32750969-T-C

48890932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32750757-T-C

48890983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32750702-G-A

48891354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32750175-C-G

48891354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32750175-C-T

48891359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32750170-G-A

48891439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32750074-T-C

48891501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32750021-T-C

48891801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32749748-C-T

48891818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32749732-A-G

48891845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32749706-T-C

48892414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32749173-T-C

48893092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32748545-T-G

48893185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32748464-C-T

48893224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32748448-C-T

48893409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32748281-G-A

48893409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32748281-G-C

48893649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32748117-T-C

http://identifiers.org/hco/10/GRCh38#48893706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32748062-C-A

48893827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747941-T-G

48893890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747875-T-C

48894145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747626-T-C

48894218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747560-T-C

48894278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747501-T-A

48894337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747459-C-G

48894434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747364-T-A

48894516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747302-A-T

48894619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747205-T-A

http://identifiers.org/hco/10/GRCh38#48894712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32747118-C-A

48894846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746976-G-A

48894846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746976-G-T

48894865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746957-C-G

48895070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746768-G-A

48895073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746765-T-C

48895240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746602-C-T

48895301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746549-C-T

48895357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746519-A-G

48895473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746417-G-A

48895473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746417-G-C

48895838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746081-A-G

48895922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746023-C-T

48895926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746019-T-C

48895933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746012-C-G

48896067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745898-C-G

48896091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745874-T-C

http://identifiers.org/hco/10/GRCh38#48897117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32745650-C-A

48897316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745525-G-T

http://identifiers.org/hco/10/GRCh38#48897325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32745517-C-A

48897325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745517-C-T

48897382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745458-A-T

48897527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32745310-A-G

48897560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32745277-C-T

48897602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745236-G-A

http://identifiers.org/hco/10/GRCh38#48897689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32745145-C-A

48897689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745145-C-T

48897691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745143-G-A

48897691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745143-G-T

48898014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744874-G-A

48898022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744866-C-G

48898022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744866-C-T

48898023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744865-T-A

48898064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744830-G-A

48898064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744830-G-T

48898079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744815-C-T

48898119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744777-A-T

48898195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744699-T-C

48898323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744595-T-C

48898418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32744007-G-A

48898700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743761-A-G

48898742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743713-T-A

http://identifiers.org/hco/10/GRCh38#48898756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32743700-A-C

48898802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743655-T-C

48898815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743647-C-T

48898834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743628-G-A

48898942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743551-C-G

48899085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743413-G-A

48899179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743301-G-A

48899234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743249-T-C

48899301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743190-A-T

48899426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743079-C-T

48899487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743030-C-T

48899518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742998-T-C

48899538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742978-C-T

48899541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742975-G-T

48899550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742966-C-T

http://identifiers.org/hco/10/GRCh38#48899663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32742854-C-A

48899671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742846-G-A

48899758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742723-G-A

48899792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742679-G-C

48899800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742670-A-G

48899838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742634-C-T

48899956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742511-C-T

48899958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742509-C-T

48900006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742467-A-G

http://identifiers.org/hco/10/GRCh38#48900077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32742425-C-A

48900077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742425-C-G

48900077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742425-C-T

http://identifiers.org/hco/10/GRCh38#48900094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32742414-A-C

48900094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742414-A-G

48900105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742398-A-G

48900105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742398-A-T

http://identifiers.org/hco/10/GRCh38#48900129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32742375-C-A

48900129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742375-C-T

48900173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742332-T-C

48900194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742312-A-G

48900264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32742242-T-A

48900264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32742242-T-G

48900275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32742231-T-A

http://identifiers.org/hco/10/GRCh38#48900357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32742150-C-A

http://identifiers.org/hco/10/GRCh38#48900368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32742139-A-C

http://identifiers.org/hco/10/GRCh38#48900373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32742134-A-C

48900373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742134-A-G

48900442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742071-G-A

48900571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741990-A-G

48900767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741804-G-A

48900787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741740-C-T

48900842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741684-T-G

48900884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741641-G-A

48900884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741641-G-T

48900935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741600-A-G

48900935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741600-A-T

48901291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741086-A-G

48901334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741013-T-C

48901394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740922-A-G

http://identifiers.org/hco/10/GRCh38#48901438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32740884-A-C

48901471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740856-C-T

48901609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740736-T-C

48901682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740672-G-A

48901682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740672-G-T

http://identifiers.org/hco/10/GRCh38#48901689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32740665-C-A

48901689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740665-C-G

48901689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740665-C-T

48901708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740646-G-A

48901708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740646-G-C

http://identifiers.org/hco/10/GRCh38#48901726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32740631-C-A

48901733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740624-A-G

48901805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32740555-T-G

48901873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740487-G-A

48901876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740481-A-G

48901878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740479-C-T

http://identifiers.org/hco/10/GRCh38#48901898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32740459-A-C

48902310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739881-G-A

48902336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739861-T-A

48902348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739849-C-G

48902348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739849-C-T

48902354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739843-C-T

48902363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739836-C-T

48902661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739545-C-T

48905197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32738255-G-A

48905224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32738226-T-G

http://identifiers.org/hco/10/GRCh38#48905569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32737953-A-C

48905573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737949-T-A

http://identifiers.org/hco/10/GRCh38#48905580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32737942-A-C

48905596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737925-G-A

48905603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737918-G-A

48905623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737897-C-G

48905645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737875-C-T

48907506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737830-A-G

48907561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737779-A-G

48907561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737779-A-T

http://identifiers.org/hco/10/GRCh38#48907589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32737751-C-A

48907589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737751-C-G

48907589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737751-C-T

48907710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737656-A-G

48908020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737371-T-C

48908064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737367-A-G

48908325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737321-A-G

48908544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737082-A-G

48908544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737082-A-T

http://identifiers.org/hco/10/GRCh38#48908833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32736795-C-A

48909128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736495-T-C

48909343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736296-T-A

48909343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736296-T-C

http://identifiers.org/hco/10/GRCh38#48910043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32735999-C-A

48910043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32735999-C-T

48910187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32735857-G-A

48910187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32735857-G-T

48910217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32735826-A-G

48910308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735728-G-A

48910308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735728-G-T

http://identifiers.org/hco/10/GRCh38#48910363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32735671-C-A

48910363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735671-C-T

48910551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735509-G-A

48910551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735509-G-T

48910792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735266-G-T

http://identifiers.org/hco/10/GRCh38#48910917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32735101-C-A

48910917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735101-C-T

48910981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735036-G-T

48911281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32733137-T-C

48911363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32733068-T-C

48911363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32733068-T-G

48911547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32732898-T-C

48911666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32732782-T-C

48911863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32732610-A-G

48912206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32732275-G-A

48912401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32732099-G-A

48912832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32731730-G-C

48913132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32731475-A-G

48913416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32731200-G-A

48913416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32731200-G-T

http://identifiers.org/hco/10/GRCh38#48913524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32731092-A-C

48913664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32730952-G-A

48913707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32730909-C-G

48913707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32730909-C-T

48914207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32730406-T-A

48914267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32730328-T-C

48914339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32730259-T-C

48914339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32730259-T-G

48914425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32730178-T-G

48914445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32730164-G-T

48914513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32730098-C-T

48914556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32730039-T-C

http://identifiers.org/hco/10/GRCh38#48914782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32729823-A-C

48914782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32729823-A-G

http://identifiers.org/hco/10/GRCh38#48914883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32729728-C-A

48914883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32729728-C-G

48914883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32729728-C-T

http://identifiers.org/hco/10/GRCh38#48914993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32729572-C-A

48915044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32729509-T-C

48915257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32729322-C-T

48922912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726747-T-A

48922970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726683-A-G

48923158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726452-C-T

48923342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726320-A-G

48923686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726073-A-G

http://identifiers.org/hco/10/GRCh38#48923738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32726025-A-C

48923892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32725899-G-A

48923898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32725893-C-T

48923906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32725885-T-C

48923906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32725885-T-G

48924255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32725533-A-G

48925053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32724756-A-G

48925527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32724235-A-G

48925751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32724000-A-G

48926104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32723668-C-G

48926106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32723666-C-G

48926106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32723666-C-T

48926135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32723637-C-T

48926182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32723590-C-G

48926905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32723220-T-A

48926905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32723220-T-G

48926956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32723172-G-A

48926964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32723164-A-G

http://identifiers.org/hco/10/GRCh38#48927157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32722827-C-A

48927157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32722827-C-T

48927201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32722704-G-T

48927213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32722696-A-G

http://identifiers.org/hco/10/GRCh38#48927458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32722443-C-A

48927458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32722443-C-T

48928059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32721858-A-G

48928059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32721858-A-T

48928102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32721817-C-T

48928158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32721760-G-A

48928158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32721760-G-T

48928676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32721127-A-G

48930492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32720519-C-T

http://identifiers.org/hco/10/GRCh38#48931858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32719363-A-C

48931924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32719299-A-G

48932249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32719044-G-T

48932331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32718977-T-A

48932412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32718903-C-G

48932487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32718834-T-C

48932584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32718741-G-A

48932584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32718741-G-T

http://identifiers.org/hco/10/GRCh38#48932585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32718740-C-A

48932585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32718740-C-T

48933049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32718626-A-G

48933296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32718411-G-A

http://identifiers.org/hco/10/GRCh38#48933366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32718326-C-A

48933366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32718326-C-T

48933444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32718258-C-T

48933946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32717794-A-G

48933967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32717775-G-A

48934140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32717606-T-C

48934934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32717479-G-T

http://identifiers.org/hco/10/GRCh38#48935053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32717356-C-A

48935053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32717356-C-T

48935140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32717292-T-A

48935217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32717224-G-A

48935223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32717218-A-G

48935278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32717163-G-A

48935408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32717051-C-T

48935736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32716771-C-T

48935927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32716374-A-T

48936072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32716253-A-G

48936236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32716096-A-G

48936380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32715961-C-T

48936489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32715850-A-G

48937822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32715345-A-G

48938041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32715129-C-T

48938110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32715051-G-A

48938112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32715049-C-T

48938314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32714830-A-G

48938571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32714562-G-A

http://identifiers.org/hco/10/GRCh38#48938959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32714237-C-A

48938960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32714236-A-G

48939017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32714180-C-T

48939071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32714138-G-C

48939206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32714032-A-G

48939331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32713901-A-G

48939475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32713758-C-T

48939593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32713647-G-A

48939649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32713589-G-A

http://identifiers.org/hco/10/GRCh38#48939658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32713580-A-C

48940905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712714-G-A

48940907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712712-C-T

48940943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712676-A-G

48941004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712607-C-T

48941644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712068-C-G

48941669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712043-A-G

48941669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712043-A-T

48941707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32712005-A-G

48941771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32711944-A-G

48943051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32711239-T-G

48943261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32711030-G-T

48943262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32711029-G-T

http://identifiers.org/hco/10/GRCh38#48943269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32711022-C-A

48943269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32711022-C-T

48943288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32711001-T-A

http://identifiers.org/hco/10/GRCh38#48943479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32710809-C-A

48943479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710809-C-T

48943492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710796-G-A

48943492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710796-G-C

48943527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710775-G-T

48943535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710768-G-A

48943535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710768-G-T

48943917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710711-G-A

48943946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710693-T-G

http://identifiers.org/hco/10/GRCh38#48943959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32710680-C-A

48943959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710680-C-T

http://identifiers.org/hco/10/GRCh38#48943972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32710667-C-A

48944654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710080-C-T

48944699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32710037-T-C

48944903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32709829-G-C

48944947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32709786-C-G

http://identifiers.org/hco/10/GRCh38#48945069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32709681-C-A

48945587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32709156-G-A

48945622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32709121-T-G

48945740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron variant
orthologous variants: 32709000-C-G

48946052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32708691-G-A

48946164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32708579-A-T

48946255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32708400-T-A

http://identifiers.org/hco/10/GRCh38#48946732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32707811-C-A

48946732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707811-C-T

http://identifiers.org/hco/10/GRCh38#48946946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32707635-A-C

http://identifiers.org/hco/10/GRCh38#48946986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32707595-C-A

48946986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707595-C-G

http://identifiers.org/hco/10/GRCh38#48946988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32707593-C-A

48946988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707593-C-T

48946994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707582-A-G

48946994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707582-A-T

48946998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707578-A-G

http://identifiers.org/hco/10/GRCh38#48947039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32707566-C-A

48947061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707544-G-A

48947061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707544-G-C

48947061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707544-G-T

48947062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707543-A-G

48947125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707493-G-A

48947194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32707425-T-C

http://identifiers.org/hco/10/GRCh38#48947448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32707134-C-A

48947626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32706917-G-C

48947626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32706917-G-T

48948162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32706453-T-C

http://identifiers.org/hco/10/GRCh38#48948190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32706425-C-A

48948190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32706425-C-T

48948263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32706352-C-T

48948508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32706101-A-G

48949170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32705461-C-G

48949284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32705338-G-A

48949353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32705281-G-C

48949440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32705232-G-A

48949592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32705074-C-T

48950027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32704648-A-G

48950077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32704598-T-C

http://identifiers.org/hco/10/GRCh38#48950966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32704286-C-A

48951876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32703339-C-T

48952214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32703032-C-T

48952690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702630-G-A

48952716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702605-T-C

48952718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702603-C-G

http://identifiers.org/hco/10/GRCh38#48952742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32702578-C-A

http://identifiers.org/hco/10/GRCh38#48952756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32702564-A-C

48952756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702564-A-G

48952762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702559-T-G

48952780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702541-C-G

48952791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702530-T-G

48952916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702430-T-G

48953066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32702294-G-A

48953232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32701991-G-T

http://identifiers.org/hco/10/GRCh38#48953288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32701816-A-C

48953368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32701753-T-A

48953368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32701753-T-C

48953520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32701617-G-A

48953700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32701448-G-A

48953700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32701448-G-T

48954064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32700869-T-G

48954158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32700780-C-T

48954203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32700730-G-A

48954276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32700689-C-G

48954276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32700689-C-T

48954289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32700676-G-T

48954713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32700265-T-C

48955447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699543-C-T

48955501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699477-T-G

48955566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699420-T-A

48957129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32699198-G-C

48957288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699039-T-C

48957298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699028-G-C

48957302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699024-G-A

48957317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699009-G-A

48957317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699009-G-C

48957317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32699009-G-T

http://identifiers.org/hco/10/GRCh38#48957355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32698964-C-A

48957355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32698964-C-T

48957358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32698961-A-G

48957501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32698798-C-T

48957727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32698655-G-T

48958009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32698413-G-A

48958009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32698413-G-T

48958174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32698302-G-T

48959379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697491-T-C

48959414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697470-G-A

48959441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697444-A-G

48959604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697298-A-G

http://identifiers.org/hco/10/GRCh38#48959924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32697013-A-C

48959924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697013-A-G

http://identifiers.org/hco/10/GRCh38#48959938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32696999-C-A

48959938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696999-C-G

48959948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696989-A-T

48960098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696857-C-T

48960139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696818-G-T

48960154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696803-G-A

48960154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696803-G-C

48960154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696803-G-T

48964073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696087-T-G

48964105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696041-T-C

48966729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32695447-G-A

48966729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32695447-G-T

48966743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32695433-G-T

48968634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694221-A-G

48968634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694221-A-T

48968647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694208-G-A

48968647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694208-G-C

48968647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694208-G-T

http://identifiers.org/hco/10/GRCh38#48968662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32694191-C-A

48968662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694191-C-T

48968679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694178-G-A

48968679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32694178-G-T

http://identifiers.org/hco/10/GRCh38#48968833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32693983-C-A

48968833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32693983-C-T

48968856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32693907-G-A

48968856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32693907-G-T

http://identifiers.org/hco/10/GRCh38#48968870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32693893-C-A

48968870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32693893-C-G

48968870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32693893-C-T

http://identifiers.org/hco/10/GRCh38#48968921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32693828-C-A

48968921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32693828-C-T

48969144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32693637-G-T

48969313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693530-G-A

48969313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693530-G-T

http://identifiers.org/hco/10/GRCh38#48969374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32693522-C-A

48969374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693522-C-T

48969425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693494-C-T

48969615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693306-G-A

http://identifiers.org/hco/10/GRCh38#48969887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32693148-C-A

48969887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693148-C-G

48969887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693148-C-T

48969890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693145-G-T

48969985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693026-T-C

http://identifiers.org/hco/10/GRCh38#48970023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32693002-C-A

48970023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693002-C-T

48970093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32692966-G-A

48970093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32692966-G-C

48970093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32692966-G-T

48970113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32692952-C-T

48970158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32692909-G-T

48970188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32692879-C-T

48972305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32692038-A-G

http://identifiers.org/hco/10/GRCh38#48972344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32692001-A-C

48972394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32691950-C-T

48972673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32691639-T-C

48972701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32691607-C-T

48972852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32691455-A-G

48972919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32691373-G-T

48973327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690928-T-C

48973418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690841-G-C

48973460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690798-G-A

48973591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690666-C-T

48973755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690539-G-T

48973809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690506-C-T

48974487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689909-A-T

48974488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689908-G-A

48974612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689836-G-T

48974717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689746-G-A

48974717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689746-G-T

http://identifiers.org/hco/10/GRCh38#48974727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32689736-C-A

48974727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689736-C-T

48974745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689718-A-T

48974775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689688-G-A

48974775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689688-G-T

48974796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689673-G-A

48974796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689673-G-T

48974797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689672-T-C

48974823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689651-T-C

48974823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689651-T-G

48974835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689639-T-C

48974916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32689553-A-G

48974989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32689480-G-A

48974989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32689480-G-C

48974989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32689480-G-T

http://identifiers.org/hco/10/GRCh38#48974996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32689473-C-A

48974996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32689473-C-T

48975090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689361-T-A

48975090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689361-T-C

48975155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689295-G-A

48975155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689295-G-T

48976294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689170-A-G

48976469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689011-G-A

48976469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689011-G-T

http://identifiers.org/hco/10/GRCh38#48976471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32689009-C-A

48976471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689009-C-T

48976506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688974-G-A

48976506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688974-G-T

48976514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688966-G-T

http://identifiers.org/hco/10/GRCh38#48976518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32688962-A-C

48976518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688962-A-G

48976926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32688372-G-A

48977009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32688288-T-C

http://identifiers.org/hco/10/GRCh38#48977033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32688266-C-A

48977039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32688260-T-C

48977040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32688259-C-G

48977040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32688259-C-T

http://identifiers.org/hco/10/GRCh38#48977047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32688252-C-A

48977047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32688252-C-T

48977105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32688194-A-G

48977105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32688194-A-T

http://identifiers.org/hco/10/GRCh38#48977124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32688176-C-A

48977134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688166-T-G

48977424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32687890-C-G

48977424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32687890-C-T

48977443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32687871-A-G

48977701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32687121-T-G

http://identifiers.org/hco/10/GRCh38#48978102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32686782-A-C

http://identifiers.org/hco/10/GRCh38#48978158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32686727-C-A

48978172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686721-A-G

http://identifiers.org/hco/10/GRCh38#48978222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32686671-C-A

48978222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686671-C-T

48978263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686629-G-T

48978288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686604-A-G

http://identifiers.org/hco/10/GRCh38#48978432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32686468-C-A

48978432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686468-C-T

http://identifiers.org/hco/10/GRCh38#48978434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32686466-C-A

48978434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686466-C-G

48978434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686466-C-T

http://identifiers.org/hco/10/GRCh38#48978437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32686463-C-A

48978437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686463-C-T

http://identifiers.org/hco/10/GRCh38#48978445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32686455-A-C

48978445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686455-A-G

48978445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686455-A-T

48978463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686437-T-C

48978525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685331-G-T

48978528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685328-A-G

http://identifiers.org/hco/10/GRCh38#48978639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32685226-C-A

http://identifiers.org/hco/10/GRCh38#48978658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32685207-A-C

48978658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685207-A-G

http://identifiers.org/hco/10/GRCh38#48978706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32685160-C-A

48978717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685146-G-T

http://identifiers.org/hco/10/GRCh38#48978739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32685123-C-A

48978771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32685080-A-T

48978776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32685075-G-T

http://identifiers.org/hco/10/GRCh38#48978807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32685043-C-A

http://identifiers.org/hco/10/GRCh38#48978809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32685041-C-A

48978809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32685041-C-T

48978844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32685010-C-T

48979036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684846-G-T

48979042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684840-A-G

48979088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684793-T-C

48979144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684743-A-G

48979334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684582-A-G

48979783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32684350-A-G

48979874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32684266-A-G

48979963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32684181-T-C

48979986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32684164-T-C

48980020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32684131-G-T

http://identifiers.org/hco/10/GRCh38#48980075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32684077-C-A

48980099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32684052-G-A

48980099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32684052-G-C

48980099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32684052-G-T

http://identifiers.org/hco/10/GRCh38#48980127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32684013-C-A

48980471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32683686-A-G

48980553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32683605-A-T

48980722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32683458-G-A

48980809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32683367-C-T

48981190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32682984-A-G

48981291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32682885-G-A

48981291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32682885-G-T

48981465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32682710-C-T

http://identifiers.org/hco/10/GRCh38#48981544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32682620-C-A

http://identifiers.org/hco/10/GRCh38#48981559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32682592-C-A

48981559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32682592-C-G

48981559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32682592-C-T

48981884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682330-T-C

48981888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682326-G-A

48981995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682249-C-G

48982009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682235-G-T

48982128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682127-G-A

48982208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682123-G-A

48982409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682059-G-A

48982409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682059-G-T

48982583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681885-G-A

48982583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681885-G-T

48982621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681827-G-T

48982630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681817-A-T

http://identifiers.org/hco/10/GRCh38#48982711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32681739-C-A

48982711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32681739-C-T

http://identifiers.org/hco/10/GRCh38#48982720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32681730-C-A

48982720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32681730-C-T

http://identifiers.org/hco/10/GRCh38#48982722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32681728-C-A

48982722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681728-C-T

48982749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681701-T-C

48982797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681668-G-A

48982813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32681654-G-C