127815114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32572043-G-A

127815114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32572043-G-T

127815138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32572025-G-T

127815201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571991-T-C

127815201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571991-T-G

127815264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571929-G-A

127815264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571929-G-C

127815264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571929-G-T

127815507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571727-A-G

127815555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571700-G-A

127815555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571700-G-T

http://identifiers.org/hco/9/GRCh38#127815598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32571680-C-A

127815598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571680-C-T

127815624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571653-G-A

127815624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571653-G-T

127815679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571574-G-A

127815679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3 prime UTR variant
orthologous variants: 32571574-G-T

http://identifiers.org/hco/9/GRCh38#127815856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32571408-C-A

127815856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32571408-C-G

127815856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32571408-C-T

http://identifiers.org/hco/9/GRCh38#127815859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32571405-C-A

127815859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32571405-C-G

127815868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32571396-T-C

127815868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32571396-T-G

127815969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: missense variant
orthologous variants: 32571281-G-A

127815969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: missense variant
orthologous variants: 32571281-G-T

http://identifiers.org/hco/9/GRCh38#127816084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32571170-A-C

http://identifiers.org/hco/9/GRCh38#127816110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32571145-C-A

127816110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32571145-C-T

http://identifiers.org/hco/9/GRCh38#127816151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32571107-C-A

127816218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32571060-G-C

http://identifiers.org/hco/9/GRCh38#127816368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32570949-A-C

127816419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570896-T-A

127816419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570896-T-C

http://identifiers.org/hco/9/GRCh38#127816477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32570842-C-A

127816477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570842-C-T

http://identifiers.org/hco/9/GRCh38#127816677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32570711-A-C

127816677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570711-A-G

127816695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570692-A-G

127816726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570662-T-A

127816726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570662-T-C

127816726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570662-T-G

127816795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570582-G-A

127816795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570582-G-T

http://identifiers.org/hco/9/GRCh38#127816840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32570536-C-A

127817282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570205-G-A

127817282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570205-G-T

http://identifiers.org/hco/9/GRCh38#127817283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32570204-C-A

127817283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570204-C-T

127817299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570194-G-T

127817315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570180-T-C

127817332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570163-G-A

127817332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32570163-G-T

127817360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570134-C-G

http://identifiers.org/hco/9/GRCh38#127817397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32570100-C-A

127817397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570100-C-T

127817463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570072-A-G

127817494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570043-G-C

127817637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569919-T-C

127817637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569919-T-G

http://identifiers.org/hco/9/GRCh38#127817788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32569726-A-C

127817788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32569726-A-G

127817795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32569721-T-C

127817795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32569721-T-G

127817810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32569706-G-A

127817810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32569706-G-T

127817876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569616-G-T

127818142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32569136-G-A

127818142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32569136-G-T

127818393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32568885-G-A

127818393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32568885-G-T

127818406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568872-T-A

127818406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568872-T-C

127818415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568863-G-A

127818415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568863-G-T

http://identifiers.org/hco/9/GRCh38#127818421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32568857-C-A

http://identifiers.org/hco/9/GRCh38#127818430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32568845-C-A

127818550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568738-A-G

127818553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568735-G-T

127818566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568728-G-A

127818566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568728-G-C

127818566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568728-G-T

http://identifiers.org/hco/9/GRCh38#127818579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32568715-C-A

127818579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568715-C-T

127818667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32568619-G-A

127818707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32568591-G-A

127818707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32568591-G-T

127819270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568354-G-T

127819312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568311-A-T

127819348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568277-A-G

127819359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568266-A-G

127819448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568158-G-C

127819448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568158-G-T

127819486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568120-G-A

127819486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568120-G-T

127819488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568118-G-C

127819488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568118-G-T

127819496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568110-G-A

127819496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568110-G-T

127819509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568097-C-T

127819518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568088-T-C

127819551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568044-G-C

127819560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568035-G-A

http://identifiers.org/hco/9/GRCh38#127819570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32568025-C-A

127819570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32568025-C-T

127819600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32567995-A-G

127819609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32567984-C-T

127819680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567913-G-A

127819726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567868-A-G

127819739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567860-C-T

127819744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567855-G-A

127819744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567855-G-T

127819781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567825-T-G

127819799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567798-C-G

127819799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567798-C-T

http://identifiers.org/hco/9/GRCh38#127819807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32567790-C-A

127819857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567743-C-T

127819872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567728-C-T

127819909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32567691-G-A

127819909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32567691-G-C

127820058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567539-A-G

http://identifiers.org/hco/9/GRCh38#127824252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32563796-A-C

http://identifiers.org/hco/9/GRCh38#127824274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32563774-C-A

127824380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32563668-T-C

127824427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: synonymous variant
orthologous variants: 32563621-T-C

127824573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32563559-C-T

127824693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32563529-G-T

http://identifiers.org/hco/9/GRCh38#127824714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32563518-A-C

127824714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32563518-A-G

http://identifiers.org/hco/9/GRCh38#127824887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#32563347-C-A

127824964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: missense variant
orthologous variants: 32563270-T-A

127824996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32563237-G-T

127825073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32563172-C-T

127825111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32563112-C-T

http://identifiers.org/hco/9/GRCh38#127825143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32563070-A-C

127825143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, undefined
orthologous variants: 32563070-A-T

127825180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32563026-C-T

http://identifiers.org/hco/9/GRCh38#127825209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32562995-C-A

127825339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: synonymous variant
orthologous variants: 32562865-C-T

127825363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 32562838-G-T

127825758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: missense_variant, undefined
orthologous variants: 32562330-A-G

127825758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: stop_gained, undefined
orthologous variants: 32562330-A-T

127825808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 32562280-G-A

127825808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 32562280-G-C

http://identifiers.org/hco/9/GRCh38#127825809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32562279-C-A

127825809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32562279-C-T

127825863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32562225-G-A

127825863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32562225-G-C

127825863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32562225-G-T

http://identifiers.org/hco/9/GRCh38#127825929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32562191-C-A

127825929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32562191-C-T

127825945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562176-T-C

127825962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562158-C-T

127825980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562140-G-A

127825980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562140-G-C

127825980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562140-G-T

127826290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561767-G-A

127826352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561661-T-A

127826605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32561422-T-G

http://identifiers.org/hco/9/GRCh38#127826622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32561402-C-A

127826622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32561402-C-T

127826785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561300-G-T

127826807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561276-T-G

127826900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561171-T-C

http://identifiers.org/hco/9/GRCh38#127826919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32561152-A-C

127826919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561152-A-G

127827021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561070-G-A

127827021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561070-G-T

http://identifiers.org/hco/9/GRCh38#127827218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32560906-A-C

http://identifiers.org/hco/9/GRCh38#127827290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32560838-C-A

127827290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560838-C-T

127827468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560312-A-G

127829747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32559513-A-G

127829748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32559512-C-G

127829748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32559512-C-T

http://identifiers.org/hco/9/GRCh38#127829767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#32559493-C-A

127829775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 32559485-C-T

127829836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32559424-C-T

127829892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32559383-C-T

127829909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32559361-G-A

127829909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32559361-G-T

127829921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32559351-C-G

127830756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32558503-A-G

127830780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32558480-A-G

http://identifiers.org/hco/9/GRCh38#127833549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32558095-C-A

http://identifiers.org/hco/9/GRCh38#127833550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32558094-A-C

127833550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32558094-A-G

127833695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557948-G-T

127833839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557803-T-A

127833839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557803-T-C

http://identifiers.org/hco/9/GRCh38#127833844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32557797-A-C

127835672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32556044-G-A

127836264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32555448-C-T

127836545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32555186-T-A

127838183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32552345-A-G

127838338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32552189-C-T

127838548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32552019-A-G

127838731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32551847-G-A

127838988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32551504-A-G

127839233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32550984-C-T

http://identifiers.org/hco/9/GRCh38#127839340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32550883-C-A

127839340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32550883-C-T

127840654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32550041-C-G

127840667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32550028-A-G

http://identifiers.org/hco/9/GRCh38#127840849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32549696-A-C

127840920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549619-T-A

http://identifiers.org/hco/9/GRCh38#127841007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32549545-C-A

127841007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549545-C-T

127841073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549475-G-A

127841073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549475-G-C

127841081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549467-T-C

127841118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32549446-T-C

127841282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549364-A-G

127841327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549317-G-C

127841327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549317-G-T

127841347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32549298-G-A

127842021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32548718-A-G

127842853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32547883-T-C

127842942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32547804-G-T

127842999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32547754-C-T

127843046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32547723-T-C

127843046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32547723-T-G

127843127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 32547647-A-G

127843258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32547516-C-T

http://identifiers.org/hco/9/GRCh38#127844596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32546526-A-C

127845368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32545713-C-T

127845521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32545564-C-T

127846402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32545143-T-C

127846427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32545118-A-G

127846787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32544786-C-G

127846852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32544700-A-G

http://identifiers.org/hco/9/GRCh38#127846863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32544689-C-A

127847051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544569-A-G

127847055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544565-T-C

127847068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544552-T-C

127847090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544533-G-A

127847090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544533-G-T

127847096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544527-G-A

127847096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544527-G-T

127847155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544473-T-C

127847170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544458-G-A

127847170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32544458-G-T

127847249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32544396-G-A

127847249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32544396-G-T

127850172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32541175-A-T

127850180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32541167-A-G

127850545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32540710-G-A

127850741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32540506-G-A

127850825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32540439-G-A

127850983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32540298-C-T

127851123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32540035-G-A

127851321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32539830-G-A

127852982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32538101-C-T

127853070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32538015-C-T

127853135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32537983-C-T

127853266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32537884-G-A

127854094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: intron variant
orthologous variants: 32537230-G-A

127854377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32536946-G-A

127854377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32536946-G-T

127854403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5 prime UTR variant
orthologous variants: 32536920-G-A

127854403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5 prime UTR variant
orthologous variants: 32536920-G-T

127854586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32536738-G-T

127854611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3349
most severe consequence: 5 prime UTR variant
orthologous variants: 32536713-G-A