52836260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30600421-T-A

http://identifiers.org/hco/3/GRCh38#52836271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30600418-C-A

52836278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30600411-T-C

http://identifiers.org/hco/3/GRCh38#52836556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30600258-C-A

52836556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30600258-C-T

http://identifiers.org/hco/3/GRCh38#52836647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30600183-C-A

52836647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30600183-C-G

52836905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599914-T-A

52836905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599914-T-C

http://identifiers.org/hco/3/GRCh38#52837023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30599788-C-A

52837023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599788-C-T

52837251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599503-T-A

52837251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599503-T-C

52837251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599503-T-G

52837262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599493-G-T

52837360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599397-G-A

52837453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599293-G-A

52837458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599288-G-T

52837526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599236-T-C

52837539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599226-C-T

52837598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599165-T-C

52837655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30599079-T-C

http://identifiers.org/hco/3/GRCh38#52837666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30599068-C-A

http://identifiers.org/hco/3/GRCh38#52837757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30598976-C-A

52837757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598976-C-T

52837837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598871-A-G

52837958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598744-C-T

52838042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598671-A-G

http://identifiers.org/hco/3/GRCh38#52838056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30598641-C-A

52838085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598614-G-A

52838085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598614-G-T

52838120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598582-T-C

52838125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598577-G-C

52838125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598577-G-T

http://identifiers.org/hco/3/GRCh38#52838126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30598576-A-C

52838126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598576-A-G

52838126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598576-A-T

52838150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598552-G-C

52838192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598515-C-T

52838213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598497-G-C

52838213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598497-G-T

http://identifiers.org/hco/3/GRCh38#52838254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30598458-A-C

52838292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598425-G-A

52838292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598425-G-C

52838292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598425-G-T

52838428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598286-G-A

52838428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598286-G-T

http://identifiers.org/hco/3/GRCh38#52838602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30598157-C-A

52838611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598148-C-T

52838615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598144-A-G

52838703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30598048-T-C

52838942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597834-A-G

52838942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597834-A-T

http://identifiers.org/hco/3/GRCh38#52839011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30597785-C-A

http://identifiers.org/hco/3/GRCh38#52839012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30597784-C-A

52839012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597784-C-T

http://identifiers.org/hco/3/GRCh38#52839038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30597758-A-C

52839038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597758-A-G

52839048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597749-G-T

http://identifiers.org/hco/3/GRCh38#52839055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30597742-C-A

52839055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597742-C-T

http://identifiers.org/hco/3/GRCh38#52839102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30597721-C-A

52839102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597721-C-T

52839188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597642-T-C

52839198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597632-G-A

52839198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597632-G-T

52839380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597478-G-T

http://identifiers.org/hco/3/GRCh38#52839390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30597455-C-A

52839390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597455-C-T

52839569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597296-C-T

52839665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597228-T-C

52839666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597227-T-A

52839770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597118-G-A

52839770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597118-G-T

52839882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597007-T-A

52839882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30597007-T-C

http://identifiers.org/hco/3/GRCh38#52840072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30596817-C-A

52840072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30596817-C-T

52840080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30596809-T-C

52840080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30596809-T-G

52840132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30596758-T-C

52840192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30596711-T-A

52840192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30596711-T-C

52840192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30596711-T-G

http://identifiers.org/hco/3/GRCh38#52840274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30596630-A-C

52840274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596630-A-G

52840274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596630-A-T

52840362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596545-G-A

52840362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596545-G-T

52840384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596523-G-T

52840414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596493-G-A

52840414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596493-G-T

52840417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596490-A-G

52840417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30596490-A-T

52841360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30595974-G-A

52841360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30595974-G-C

52841439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595911-G-A

http://identifiers.org/hco/3/GRCh38#52841552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30595800-C-A

52841552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595800-C-G

52841552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595800-C-T

52841578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595774-C-T

52841966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595532-C-G

52841966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595532-C-T

52842032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595475-C-G

52842032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595475-C-T

52842071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595440-C-T

52842093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595417-T-A

52842093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595417-T-C

52842153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595311-A-G

52842285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595096-A-G

http://identifiers.org/hco/3/GRCh38#52842333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30595048-A-C

52842344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595038-G-A

52842344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595038-G-C

52842588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30594857-C-T

52842781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30594683-T-C

52842782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30594682-G-A

52842848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30594617-T-C

52842848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30594617-T-G

52842903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30594562-T-C

52842982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30594482-G-A

52842982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30594482-G-T

http://identifiers.org/hco/3/GRCh38#52843025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30594445-C-A

http://identifiers.org/hco/3/GRCh38#52843128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30594367-C-A

52843128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30594367-C-T

52843174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30594320-G-A

52843174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30594320-G-T

http://identifiers.org/hco/3/GRCh38#52843187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30594297-C-A

52843187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30594297-C-T

http://identifiers.org/hco/3/GRCh38#52843253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30593982-C-A

52843253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30593982-C-T

52843254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30593981-G-A

52843254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30593981-G-C

52843254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30593981-G-T

52843603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30593641-A-G

52844702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30592845-A-G

http://identifiers.org/hco/3/GRCh38#52844712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30592836-A-C

52844712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30592836-A-G

52844712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30592836-A-T

http://identifiers.org/hco/3/GRCh38#52844903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30592739-C-A

52844903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: missense variant
orthologous variants: 30592739-C-T

52844991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30592659-G-A

http://identifiers.org/hco/3/GRCh38#52845076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30592558-A-C

52845433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, undefined
orthologous variants: 30592248-C-T

http://identifiers.org/hco/3/GRCh38#52845457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30592219-A-C

52845654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591979-G-A

52845682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591946-C-T

52845715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591911-G-C

52845728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591898-G-A

52845744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591872-C-T

52845758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591858-C-T

52846068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591679-G-A

http://identifiers.org/hco/3/GRCh38#52846093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30591654-C-A

52846194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591532-C-T

52846204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591522-G-A

52846467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30591293-T-C

52846523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30591237-G-A

http://identifiers.org/hco/3/GRCh38#52846530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30591230-C-A

52846530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30591230-C-T

52846535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30591225-A-T

52846577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591177-A-G

52846691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591085-A-G

http://identifiers.org/hco/3/GRCh38#52846715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30591061-C-A

52846774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, undefined
orthologous variants: 30591007-T-C

52846776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591005-G-A

52846776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30591005-G-T

http://identifiers.org/hco/3/GRCh38#52847243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30590769-A-C

http://identifiers.org/hco/3/GRCh38#52847389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30590723-A-C

http://identifiers.org/hco/3/GRCh38#52847401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30590711-C-A

http://identifiers.org/hco/3/GRCh38#52847452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30590660-A-C

52847452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30590660-A-G

52847452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 30590660-A-T

http://identifiers.org/hco/3/GRCh38#52847583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30590551-A-C

52847618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30590521-T-A

52847618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30590521-T-G

http://identifiers.org/hco/3/GRCh38#52847652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30590502-C-A

52847671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30590483-A-G

52847687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30590467-T-C

52848026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30590154-G-A

52848210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589998-G-A

http://identifiers.org/hco/3/GRCh38#52848276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30589926-A-C

52848380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589842-G-T

52848388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589831-A-G

http://identifiers.org/hco/3/GRCh38#52848443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30589791-A-C

52848443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589791-A-G

http://identifiers.org/hco/3/GRCh38#52848444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30589790-C-A

52848444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589790-C-G

52848444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589790-C-T

http://identifiers.org/hco/3/GRCh38#52848477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30589768-C-A

52848477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589768-C-T

52848551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30589725-T-C

52848645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30589630-T-C

52848695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30589591-T-A

52848724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30589562-T-C

52848781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30589503-C-T

52849322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30589094-C-T

52849351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30589065-G-A

http://identifiers.org/hco/3/GRCh38#52849572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30588877-A-C

http://identifiers.org/hco/3/GRCh38#52849645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30588804-C-A

52849645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588804-C-G

http://identifiers.org/hco/3/GRCh38#52849660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30588788-C-A

52849660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588788-C-G

52849660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588788-C-T

http://identifiers.org/hco/3/GRCh38#52849739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30588741-C-A

52849739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588741-C-T

52850029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588457-T-C

52850029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588457-T-G

52850175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588408-C-G

52850480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588303-G-A

52850480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588303-G-T

52850498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588285-T-C

http://identifiers.org/hco/3/GRCh38#52850541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30588243-C-A

52850680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30588104-A-G

52851044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30587940-G-A

52851337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30587668-T-G

52851469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30587536-C-T

52851522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30587496-A-T

52852423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30586636-A-G

52852451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30586609-T-C

52852451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30586609-T-G

52852580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: intron variant
orthologous variants: 30586502-G-A

52853821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30586045-T-A

52853852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30586016-T-C

http://identifiers.org/hco/3/GRCh38#52855347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30584935-C-A

52855347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584935-C-T

52855376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584903-A-T

http://identifiers.org/hco/3/GRCh38#52855491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30584790-A-C

52855491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584790-A-G

52855727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584574-G-A

52855922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584401-C-T

52855923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584400-G-A

52856096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584292-G-T

52856114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584283-A-G

52856125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584272-G-T

52856272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584136-T-C

52856327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30584082-C-T

52856826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583873-A-G

52856972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583748-C-G

52857075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583648-G-T

52857102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583626-G-A

52857155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583576-G-C

52857155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583576-G-T

52857332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30583399-C-T

52857695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582970-T-C

52857756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582893-A-G

52857807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582853-G-C

52857906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30582805-T-C

52862541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30579607-T-C

52862575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30579573-A-G

52871072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30579283-T-G

http://identifiers.org/hco/3/GRCh38#52871448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30578910-C-A

52872024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30578298-C-T

52872309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30578036-G-A

52875009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30569582-C-T

52875061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30569537-G-A

52875129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30569448-G-C

http://identifiers.org/hco/3/GRCh38#52875365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30568677-C-A

52875365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568677-C-G

52875476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568579-C-T

52875539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568528-T-C

52875753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568326-T-C

http://identifiers.org/hco/3/GRCh38#52875770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30568311-A-C

52875771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30568310-T-C

http://identifiers.org/hco/3/GRCh38#52876018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30568057-C-A

52876441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567698-C-T

52876917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567517-G-T

52877184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567283-T-G

52877315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567164-T-C

52877315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567164-T-G

52877346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567134-A-G

52877378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30567098-G-A

http://identifiers.org/hco/3/GRCh38#52879058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30566850-A-C

52879203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566715-G-A

52879500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566452-G-A

52879552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566407-A-G

52879596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566377-G-A

52879704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566325-G-A

52879704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30566325-G-C

52880254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30565888-G-A

52880758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30564942-G-A

52880767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30564929-A-G

52880767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30564929-A-T

52880862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30564874-A-G

52885681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30559649-C-T

52885770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30559623-C-T

52885785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30559612-T-C

52885803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30559594-G-T

52886034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30559377-C-T

52886237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30559216-G-A

http://identifiers.org/hco/3/GRCh38#52886533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30558986-A-C

52886982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30558493-G-C

52887446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30558039-G-T

52887470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30558013-G-A

52887470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30558013-G-C

52887475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30558010-C-T

52887552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30557937-C-T

52887580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30557914-C-T

52887772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30557696-C-T

52887898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30557472-T-C

52888497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30556843-G-C

http://identifiers.org/hco/3/GRCh38#52888568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30556810-C-A

52888568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30556810-C-T

52888717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30556671-G-A

52888769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30556624-T-G

52888777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30556616-T-C

52888777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30556616-T-G

52888845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30556542-G-A

http://identifiers.org/hco/3/GRCh38#52888999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30556345-C-A

52890497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30555154-T-C

52890551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30555105-A-G

52890656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30555006-A-G

http://identifiers.org/hco/3/GRCh38#52890681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30554987-A-C

52890681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554987-A-T

52890791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554898-T-C

52891083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554376-A-G

52891114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554257-A-T

52891179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554137-G-C

52891198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554087-G-A

52891198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30554087-G-T

52891422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553847-C-T

52891483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553786-T-C

52891490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553779-G-C

http://identifiers.org/hco/3/GRCh38#52891510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30553758-A-C

52891511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553757-C-T

52891598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553669-C-T

52891657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553598-G-C

52891679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553576-T-C

52891830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553417-A-G

52891855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30553394-C-T

52891896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30553350-T-C

52891961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30553289-T-C

52892687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30552697-T-C

52892736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30552644-T-C

52893038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30552312-G-A

52893317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551909-G-A

http://identifiers.org/hco/3/GRCh38#52893358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30551868-C-A

52893454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551799-T-G

52893455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551798-T-C

52893584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551681-G-T

52893879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551316-C-T

52893894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30551304-T-A

52894157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30551065-T-C

52894274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30550935-C-T

52894826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30550433-C-T

52894948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30550335-G-T

52895199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549883-C-T

http://identifiers.org/hco/3/GRCh38#52895216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30549866-A-C

52895301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549784-G-A

52895301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549784-G-C

52895415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549722-C-T

52895939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 30549218-G-C

http://identifiers.org/hco/3/GRCh38#52895946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30549211-C-A

52895946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 30549211-C-T

52895975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549182-T-C

52895975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549182-T-G

52896030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549148-G-C

52896134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30549058-G-A

52896877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30548290-G-A

52896877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30548290-G-C

52897050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30548101-T-C

http://identifiers.org/hco/3/GRCh38#52897255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30547879-C-A

52897255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30547879-C-T

http://identifiers.org/hco/3/GRCh38#52897263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30547871-C-A

52897263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30547871-C-T

52897268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30547866-G-A

52897268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30547866-G-C

52897268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30547866-G-T

52897380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 30547756-G-A

52897380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 30547756-G-C

52897380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 30547756-G-T

http://identifiers.org/hco/3/GRCh38#52897425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30547711-C-A

52897501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30526
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 30547645-T-C