http://identifiers.org/hco/2/GRCh38#69321161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87069593-C-A

69321267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87069489-A-G

69321319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87069434-C-T

http://identifiers.org/hco/2/GRCh38#69321353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87069409-C-A

69321900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068827-A-G

http://identifiers.org/hco/2/GRCh38#69321912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87068815-C-A

69321999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068746-C-T

http://identifiers.org/hco/2/GRCh38#69322098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87068646-C-A

69322228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068508-T-C

http://identifiers.org/hco/2/GRCh38#69322262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87068474-C-A

69322273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068466-T-C

69322333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068390-G-A

69322333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068390-G-T

http://identifiers.org/hco/2/GRCh38#69322407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87068311-A-C

69322510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068258-C-G

69322510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068258-C-T

http://identifiers.org/hco/2/GRCh38#69322556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87068237-C-A

69322751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87068064-T-C

69322918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87067942-T-C

69322927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87067934-A-G

69323037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87067858-G-A

69323117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87067787-T-C

http://identifiers.org/hco/2/GRCh38#69323118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87067786-A-C

http://identifiers.org/hco/2/GRCh38#69323158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87067764-C-A

69323172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87067750-C-G

69323174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87067748-T-C

69323191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87067731-G-A

http://identifiers.org/hco/2/GRCh38#69323332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87067251-C-A

69324551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87066594-C-T

http://identifiers.org/hco/2/GRCh38#69324650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87066539-C-A

69324788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87066433-C-T

69324931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87066295-A-G

69324942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87066284-A-G

69325138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87066109-G-A

69325300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065954-T-A

http://identifiers.org/hco/2/GRCh38#69325470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87065790-C-A

69325470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065790-C-T

69325535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065734-G-A

69325607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065696-T-C

http://identifiers.org/hco/2/GRCh38#69325698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87065621-C-A

69325698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065621-C-G

69325738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065573-C-T

69325750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065561-T-C

69325791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065527-T-C

69326044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065272-G-A

69326044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3 prime UTR variant
orthologous variants: 87065272-G-T

69326196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: missense variant
orthologous variants: 87065131-A-T

69326501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064968-C-T

69326544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064926-G-A

69326553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064917-G-T

69326572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064898-T-C

69326572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064898-T-G

69326711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064798-G-A

69326776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064751-G-A

69326776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064751-G-T

69326801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064725-A-G

69326801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064725-A-T

69326815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064708-G-A

69326815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064708-G-T

http://identifiers.org/hco/2/GRCh38#69326838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87064636-A-C

69326862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064606-T-A

69326862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064606-T-C

69327115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064261-G-A

69327115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064261-G-T

http://identifiers.org/hco/2/GRCh38#69327157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87064224-A-C

69327157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87064224-A-G

69327420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87063999-A-G

69327721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87063680-A-G

69327741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87063660-G-A

http://identifiers.org/hco/2/GRCh38#69329500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87062163-A-C

69329507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87062155-G-A

69329655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87062016-A-G

69329655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87062016-A-T

69329686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 87059565-G-A

69329686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 87059565-G-T

69333704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87056700-A-G

69333792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87056616-G-A

69334311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87056445-T-G

69334347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87056406-C-T

69335496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87055300-C-T

69335749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87055081-G-T

69336929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87054836-G-C

http://identifiers.org/hco/2/GRCh38#69336970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87054800-A-C

69338116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87054007-G-T

http://identifiers.org/hco/2/GRCh38#69338150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87053971-A-C

69338323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87053647-T-C

69338414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87053386-C-T

69338422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87053378-T-A

69338422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87053378-T-C

http://identifiers.org/hco/2/GRCh38#69338667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87053157-A-C

69338746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87052982-A-T

69338972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87052888-G-A

69339076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87052810-G-A

69339076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87052810-G-T

69339107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87052775-T-C

69339265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87052659-A-G

69339458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87052479-T-C

69339749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87051863-G-A

69339756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87051851-T-G

69341534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050657-A-G

http://identifiers.org/hco/2/GRCh38#69341619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87050599-C-A

69341651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050569-A-G

69342098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050516-G-T

http://identifiers.org/hco/2/GRCh38#69342124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87050488-C-A

69342124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050488-C-T

69342153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 87050458-G-T

69342339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050272-G-A

69342339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050272-G-T

69342370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050240-T-G

69342492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050168-A-G

69342546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87050123-G-C

69342710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87049967-T-C

69342710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87049967-T-G

69345678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044942-G-A

69345730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044895-T-G

http://identifiers.org/hco/2/GRCh38#69345811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87044846-C-A

69345830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044825-G-A

69345830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044825-G-C

69345830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044825-G-T

69345835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044820-T-G

http://identifiers.org/hco/2/GRCh38#69345856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87044799-C-A

69345886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044775-T-A

69345912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: missense variant
orthologous variants: 87044751-T-C

http://identifiers.org/hco/2/GRCh38#69345948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87044715-A-C

69346013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044650-A-G

69346013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044650-A-T

69346018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044645-C-T

69346123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87044514-A-T

69347937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043979-T-C

69348002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043911-A-G

69348005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043908-A-T

69348044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043874-G-A

69348044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043874-G-T

http://identifiers.org/hco/2/GRCh38#69348116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87043819-A-C

69348116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043819-A-G

69348116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043819-A-T

69348117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043818-G-C

69348117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043818-G-T

http://identifiers.org/hco/2/GRCh38#69348486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87043285-A-C

69348611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87043156-G-A

69348830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87042944-T-C

69349828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87041172-G-A

69349867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87041138-T-C

69349871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87041134-T-C

http://identifiers.org/hco/2/GRCh38#69349942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87041070-A-C

69350055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87040913-T-C

http://identifiers.org/hco/2/GRCh38#69350277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87040688-C-A

69350943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87040236-T-A

69350943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87040236-T-G

69354446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037629-A-G

69354460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037615-C-T

69354479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037597-G-C

69354479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037597-G-T

69354596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037477-A-G

69354596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037477-A-T

http://identifiers.org/hco/2/GRCh38#69354637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87037433-A-C

69354641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037404-G-A

69354641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037404-G-T

69354668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87037378-T-A

http://identifiers.org/hco/2/GRCh38#69354674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87037372-C-A

69355842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87036713-T-C

http://identifiers.org/hco/2/GRCh38#69355846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87036709-A-C

69355846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87036709-A-T

69355870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87036686-A-G

http://identifiers.org/hco/2/GRCh38#69356343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87036548-C-A

http://identifiers.org/hco/2/GRCh38#69356592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87036324-A-C

69356625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87036293-C-G

69356654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87036265-C-T

http://identifiers.org/hco/2/GRCh38#69356662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87036258-C-A

http://identifiers.org/hco/2/GRCh38#69356689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87036232-C-A

69356689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87036232-C-T

http://identifiers.org/hco/2/GRCh38#69358271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87035197-C-A

69358411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: missense variant
orthologous variants: 87034662-T-C

69358486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87034584-G-T

69358680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033743-T-C

http://identifiers.org/hco/2/GRCh38#69359171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87033259-C-A

69359171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033259-C-T

69359230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033220-T-A

69359230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033220-T-C

69359238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033212-A-G

69359238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033212-A-T

69359241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033209-G-A

69359241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033209-G-T

69359242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033208-G-A

69359242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033208-G-C

69359242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033208-G-T

69359245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87033205-T-C

69359260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 87033190-T-C

69359260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 87033190-T-G

69359526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87032772-T-C

69359633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87032690-T-C

http://identifiers.org/hco/2/GRCh38#69359968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87032369-A-C

69360017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87032320-G-A

69360017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87032320-G-T

http://identifiers.org/hco/2/GRCh38#69363413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87031837-C-A

69363496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87031754-A-G

69363528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: intron variant
orthologous variants: 87031723-A-G

69363663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87031588-T-C

69363663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87031588-T-G

69363704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87031547-A-G

69369763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87031011-G-A

69369899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87030889-A-T

69370207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87030628-C-G

69370211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87030624-T-A

69370438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87030316-C-T

69370449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87030305-A-T

http://identifiers.org/hco/2/GRCh38#69370466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87030294-A-C

69370613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87030168-A-G

69373876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87028137-A-G

69374023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 87027991-C-T

69374136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87027884-T-C

69374205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87027820-G-T

69374216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87027809-T-C

69374420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87027699-T-G

69379474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87023613-T-C

69383255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87022827-G-C

69383497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87022400-T-C

http://identifiers.org/hco/2/GRCh38#69386019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87021428-C-A

69386019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87021428-C-T

http://identifiers.org/hco/2/GRCh38#69386050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87021330-C-A

69386482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87020895-C-G

69386598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87020783-T-C

69386886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87020274-T-G

http://identifiers.org/hco/2/GRCh38#69386926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87020226-C-A

69386953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87020169-G-T

http://identifiers.org/hco/2/GRCh38#69386977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87020145-C-A

http://identifiers.org/hco/2/GRCh38#69387022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87020079-C-A

69387022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87020079-C-T

http://identifiers.org/hco/2/GRCh38#69387030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87020064-C-A

69387030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87020064-C-G

69387030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87020064-C-T

http://identifiers.org/hco/2/GRCh38#69387115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87019948-C-A

69387115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 87019948-C-G

69387115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 87019948-C-T

http://identifiers.org/hco/2/GRCh38#69387121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87019942-C-A

69387121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 87019942-C-T

69387143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87019929-G-A

69387143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87019929-G-C

69387143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87019929-G-T

69387167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87019909-G-A

69387167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87019909-G-T

69387203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 87019874-G-A

69387203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 87019874-G-T

http://identifiers.org/hco/2/GRCh38#69387241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87019839-C-A

69387241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4241
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87019839-C-T