34865953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 3 prime UTR variant
orthologous variants: 127130289-G-A

34865953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 3 prime UTR variant
orthologous variants: 127130289-G-C

34865953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 3 prime UTR variant
orthologous variants: 127130289-G-T

34866310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129933-C-T

http://identifiers.org/hco/1/GRCh38#34866317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129926-C-A

34866317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129926-C-T

http://identifiers.org/hco/1/GRCh38#34866322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129921-C-A

34866322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129921-C-G

34866355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129875-G-A

34866355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129875-G-T

http://identifiers.org/hco/1/GRCh38#34866360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129870-C-A

34866360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129870-C-T

http://identifiers.org/hco/1/GRCh38#34866367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129863-C-A

34866367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129863-C-G

34866367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129863-C-T

http://identifiers.org/hco/1/GRCh38#34866370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129860-A-C

34866370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129860-A-G

34866370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129860-A-T

34866374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129856-C-T

http://identifiers.org/hco/1/GRCh38#34866418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129808-C-A

34866418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129808-C-G

34866418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129808-C-T

http://identifiers.org/hco/1/GRCh38#34866428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129798-C-A

34866430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129796-G-A

34866430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129796-G-T

http://identifiers.org/hco/1/GRCh38#34866432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129794-C-A

34866432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129794-C-T

http://identifiers.org/hco/1/GRCh38#34866439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129788-C-A

34866439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129788-C-T

34866442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129785-G-A

34866442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129785-G-T

34866458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129768-G-C

34866628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, undefined
orthologous variants: 127129619-A-G

34866824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129505-G-A

34866945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129419-T-C

34867332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129055-A-G

http://identifiers.org/hco/1/GRCh38#34867340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127129047-C-A

34867340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127129047-C-T

34867403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127128944-A-G

34867403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127128944-A-T

34867451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127128902-C-G

34867451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127128902-C-T

http://identifiers.org/hco/1/GRCh38#34867756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127128639-C-A

34867769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127128626-A-G

34867769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127128626-A-T

34867780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127128613-C-T

34868421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127971-C-G

34868421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127971-C-T

http://identifiers.org/hco/1/GRCh38#34868524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127127902-C-A

34868527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127899-G-A

34868527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127899-G-T

34868530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127896-A-T

34868540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127889-G-A

34868540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127889-G-T

http://identifiers.org/hco/1/GRCh38#34868546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127127883-C-A

34868546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127883-C-T

http://identifiers.org/hco/1/GRCh38#34868579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127127838-C-A

34868593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127824-G-T

34868799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127127616-G-A

34868799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127127616-G-T

34868801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: synonymous variant
orthologous variants: 127127614-G-C

34868801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: synonymous variant
orthologous variants: 127127614-G-T

34868889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127127526-T-C

http://identifiers.org/hco/1/GRCh38#34868973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127127442-C-A

34869015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127127400-C-T

http://identifiers.org/hco/1/GRCh38#34869051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127127364-C-A

34869051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127127364-C-G

34869077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: synonymous variant
orthologous variants: 127127338-G-A

34869077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127127338-G-T

34869095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 127127320-G-A

34869095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 127127320-G-C

http://identifiers.org/hco/1/GRCh38#34869106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127127309-C-A

34869106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127309-C-T

34869109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127306-T-A

34869109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127306-T-C

34869125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127288-A-G

34869125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127288-A-T

34869176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127219-G-A

34869176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127219-G-T

34869234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127127160-C-T

34869719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127126861-A-T

34869835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127126751-G-C

34869999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127126616-G-C

34870112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127126499-G-A

34870307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127126292-G-A

34870431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127126156-G-A

http://identifiers.org/hco/1/GRCh38#34870686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127125889-C-A

http://identifiers.org/hco/1/GRCh38#34871676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127124844-C-A

34873120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127121933-T-G

34873158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127121895-C-T

34873326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127121626-G-T

34873504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127121451-G-A

34873614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127121342-G-A

34874280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127120452-A-G

34874280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127120452-A-T

34874291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127120441-A-G

34874622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127120209-T-C

34874718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127120163-G-T

34876079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127118888-C-T

http://identifiers.org/hco/1/GRCh38#34876132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127118842-C-A

34876494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127117912-G-A

34876674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127117732-C-T

http://identifiers.org/hco/1/GRCh38#34876786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127117636-C-A

34876829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127117621-G-A

http://identifiers.org/hco/1/GRCh38#34876971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127117492-C-A

34877100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127117367-T-A

34877177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127117301-G-A

34877206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127117272-C-T

34877237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127117241-G-A

34882313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127111819-C-T

34882363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127111759-A-G

34882729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127111582-T-C

34883203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127111116-G-A

34883274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127111062-G-A

34883295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127111041-T-C

34883588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127110820-T-C

http://identifiers.org/hco/1/GRCh38#34883665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127110740-C-A

34883804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127110617-G-C

34884676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127109958-C-T

http://identifiers.org/hco/1/GRCh38#34884773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127109811-C-A

34884898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127109266-A-G

34884898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127109266-A-T

34885350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, undefined
orthologous variants: 127108909-G-A

34885350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, undefined
orthologous variants: 127108909-G-C

34885350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, undefined
orthologous variants: 127108909-G-T

http://identifiers.org/hco/1/GRCh38#34885405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127108853-C-A

34885405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108853-C-T

34885480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 127108785-G-T

34885610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: synonymous variant
orthologous variants: 127108655-T-A

34885680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127108585-G-A

34885680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127108585-G-C

34885680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127108585-G-T

34885895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108403-G-A

34885976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108351-T-A

http://identifiers.org/hco/1/GRCh38#34886055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127108330-C-A

34886055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108330-C-T

34886299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108086-G-A

34886305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108080-G-T

34886376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108008-A-G

34886382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127108002-G-A

34886499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127107925-C-T

34887755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127107280-T-C

34887897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127107143-G-A

34888153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106908-T-C

34888200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106872-T-C

34888415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106669-G-A

34888472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106630-G-A

34888498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106602-A-G

34888715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106345-A-G

34888727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106333-T-C

34888839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127106258-A-G

34889177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127105934-G-A

34889177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127105934-G-T

34889277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127105832-G-A

34889277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127105832-G-C

34889399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127105728-G-T

34889406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127105721-A-G

34889449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127105677-G-A

34890647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127104589-T-C

http://identifiers.org/hco/1/GRCh38#34890689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127104547-C-A

34890877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127104376-G-A

34890877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127104376-G-C

34897118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127097177-A-G

34897890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127096027-G-A

34897890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127096027-G-C

34897970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127095919-G-A

34898003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127095871-A-G

34898493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127095347-A-G

http://identifiers.org/hco/1/GRCh38#34898562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127095276-C-A

34898562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127095276-C-G

34899242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127094548-A-G

34899303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127094487-C-T

34899434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127094359-C-T

34899539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127094265-T-G

http://identifiers.org/hco/1/GRCh38#34899840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127093959-C-A

34899840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093959-C-T

34899854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093923-A-G

34899867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093910-G-A

34899874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093903-T-C

34899885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093848-A-G

http://identifiers.org/hco/1/GRCh38#34899888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127093845-C-A

http://identifiers.org/hco/1/GRCh38#34900003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127093725-C-A

http://identifiers.org/hco/1/GRCh38#34900010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127093718-C-A

34900010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093718-C-T

http://identifiers.org/hco/1/GRCh38#34900026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127093702-C-A

34900035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093695-G-T

34900356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093378-G-A

34900356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093378-G-T

34900418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093312-G-A

34900434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093295-C-T

34900462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093267-C-T

34900669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127093097-T-G

34900987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127092797-G-A

34901013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127092771-G-A

34901155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127092627-C-G

34901155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127092627-C-T

http://identifiers.org/hco/1/GRCh38#34901221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127092563-C-A

34901221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127092563-C-G

34901398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127092387-G-A

34901445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127092340-C-T

34901824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091958-A-G

34901850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091932-A-G

34902008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091814-G-A

34902341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091609-C-T

34902427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091532-C-T

http://identifiers.org/hco/1/GRCh38#34902508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127091301-C-A

34902531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091278-C-T

34902555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091255-C-T

34902759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127091051-G-A

34902816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127090985-G-A

http://identifiers.org/hco/1/GRCh38#34902970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127090853-C-A

34902970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127090853-C-T

34903400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127090396-T-C

34903713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127090041-G-C

34903894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127089865-T-G

34903897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127089862-C-T

34903975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127089786-T-C

34904038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127089724-G-A

34904178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127089592-A-G

34904458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127089323-T-C

34904695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127089089-T-C

34904727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: synonymous variant
orthologous variants: 127089057-G-A

34904727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: synonymous variant
orthologous variants: 127089057-G-C

34904727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: synonymous variant
orthologous variants: 127089057-G-T

34905163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127088627-T-A

34905163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense variant
orthologous variants: 127088627-T-G

34905184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127088603-T-C

34905396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127088391-G-T

http://identifiers.org/hco/1/GRCh38#34905515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127088272-C-A

34906317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127087952-C-T

34906574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127087731-C-T

34906654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127087650-C-T

34906710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127087588-T-A

http://identifiers.org/hco/1/GRCh38#34906716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127087582-C-A

34907420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127086883-G-A

34907420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127086883-G-T

http://identifiers.org/hco/1/GRCh38#34907565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127086744-C-A

34907565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127086744-C-T

34907848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127086471-G-A

34908048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127086283-C-G

34908057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127086274-C-T

34908615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127085761-G-A

34908753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127085624-G-A

34908921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127085457-T-C

34909310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

34909503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

34909693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127083532-T-A

34909822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127083411-G-C

34910155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127083082-T-A

34910522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127082751-T-A

34910805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127082456-A-T

34911488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127081573-G-A

34911491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127081570-G-C

34911592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127081481-T-G

34911942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127081131-A-G

34912102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080973-T-C

34912115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080960-A-G

34912239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080825-T-C

34912272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080791-T-C

34912445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080626-T-C

34912490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080589-C-T

http://identifiers.org/hco/1/GRCh38#34912701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127080388-C-A

34912701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080388-C-T

34913280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079839-T-A

34913508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079590-C-G

34913749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079400-C-T

http://identifiers.org/hco/1/GRCh38#34913836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127079317-C-A

http://identifiers.org/hco/1/GRCh38#34914006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127079209-A-C

34914011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079204-G-C

34914100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079108-C-T

34914140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079068-C-T

34914631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078663-G-A

34914709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078594-G-T

34914852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078455-T-C

34914883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078371-T-C

34914916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078338-C-T

34914937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078317-G-A

34915007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078249-C-G

http://identifiers.org/hco/1/GRCh38#34915070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127078185-A-C

34915771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127077520-G-A

34915792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127077492-G-A

34918464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127074009-G-A

34918720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073755-G-A

34918895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073584-G-A

http://identifiers.org/hco/1/GRCh38#34919119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127073367-C-A

34919119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073367-C-T

34919134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073351-C-T

34919141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073345-G-A

34920467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072421-T-C

34920498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072390-C-T

34920566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072284-C-G

34921180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071683-C-G

34921180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071683-C-T

34921322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071311-C-T

34921492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071021-T-C

34921538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070954-C-T

34921653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070822-T-C

34921714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070666-T-C

34921852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070474-C-T

34921876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070464-T-C

34922037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070318-C-T

34922664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127069704-A-G

34922789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127069595-G-A

34923081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127069342-T-A

34923124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127069298-G-A

34923747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127068718-A-G

34924095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127068368-G-A

34924386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127068072-C-G

34924386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127068072-C-T

34924434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127068024-G-C

34924784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127067701-G-A

34924996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127067498-G-A

34925386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127067143-A-G

34925407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127067122-G-T

http://identifiers.org/hco/1/GRCh38#34925440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127067089-C-A

34925440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127067089-C-G

34925507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127067022-A-G

http://identifiers.org/hco/1/GRCh38#34925548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127066988-C-A

34925548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127066988-C-T

34925700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127066831-T-G

34925714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127066817-G-C

34925734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127066797-A-G

34925794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127066734-T-G

34926960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127065469-G-A

34926970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127065459-C-T

http://identifiers.org/hco/1/GRCh38#34927000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127065426-C-A

34928254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127064187-C-T

34929331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127063277-G-C

34929331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127063277-G-T

34929409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127063198-G-A

34929418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: intron variant
orthologous variants: 127063189-G-A

34929577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30368
most severe consequence: 5 prime UTR variant
orthologous variants: 127063030-C-T