http://identifiers.org/hco/22/GRCh38#43879979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83996610-C-A

43879979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996610-C-T

43880026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996656-G-C

43880026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996656-G-T

43880080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996707-C-T

43880093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996714-G-A

http://identifiers.org/hco/22/GRCh38#43880146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83996745-C-A

http://identifiers.org/hco/22/GRCh38#43880197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83996786-C-A

43880197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996786-C-T

http://identifiers.org/hco/22/GRCh38#43880352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83996876-A-C

43880352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996876-A-G

43880352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996876-A-T

43880371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996898-G-A

43880371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996898-G-T

43880385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996911-C-T

43880391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996917-A-G

43880391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83996917-A-T

http://identifiers.org/hco/22/GRCh38#43880393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83996919-C-A

http://identifiers.org/hco/22/GRCh38#43880536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83997009-A-C

43880536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997009-A-G

43880536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997009-A-T

http://identifiers.org/hco/22/GRCh38#43880554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83997024-C-A

43880554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997024-C-G

43880554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997024-C-T

43880682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997180-T-A

43880682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997180-T-C

43880682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997180-T-G

43880713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997253-G-A

43880713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997253-G-T

43880728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 3 prime UTR variant
orthologous variants: 83997281-A-G

http://identifiers.org/hco/22/GRCh38#43880813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83997404-C-A

43880813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83997404-C-T

43880841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: 83997432-T-C

43880858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83997449-T-C

43880877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: 83997465-G-A

43880920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997513-G-A

43880920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997513-G-T

http://identifiers.org/hco/22/GRCh38#43881003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83997585-C-A

43881003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997585-C-T

http://identifiers.org/hco/22/GRCh38#43881344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83997799-C-A

43881365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997824-G-A

43881421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997900-A-G

43881421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997900-A-T

43881434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997913-G-A

43881434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997913-G-T

43881445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83997924-G-T

http://identifiers.org/hco/22/GRCh38#43881530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83998015-C-A

43881530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998015-C-T

43881534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998019-A-G

http://identifiers.org/hco/22/GRCh38#43881552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83998042-C-A

43881552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998042-C-T

43881556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: splice donor variant
orthologous variants: 83998046-A-G

43881556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: splice donor variant
orthologous variants: 83998046-A-T

43881602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83998092-G-A

43881602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83998092-G-C

43881656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83998146-G-A

43881656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83998146-G-T

43881695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998185-G-A

43881695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998185-G-T

http://identifiers.org/hco/22/GRCh38#43881696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83998186-C-A

43881749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998214-G-A

43881749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998214-G-T

43881768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998233-G-A

43881768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998233-G-C

43881768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998233-G-T

http://identifiers.org/hco/22/GRCh38#43881788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83998247-C-A

43881788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998247-C-T

43881855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998288-C-T

43881862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998295-G-A

43881862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998295-G-T

43881939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998367-A-G

43881948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998376-C-T

43881972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998384-T-C

43882030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998436-C-G

43882702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998646-G-A

43882730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998674-G-A

43882967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83998959-G-C

43883054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999057-C-G

43883054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999057-C-T

43883142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999144-G-A

43883247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999243-G-C

43883288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999271-T-C

43883293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999276-G-A

43883317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999297-C-G

43883317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999297-C-T

43883391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999370-T-C

43883491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999447-C-T

43883585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999512-G-A

43883952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999627-T-A

43883952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999627-T-C

43884025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999676-T-C

43884065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999718-G-A

43884065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999718-G-T

43884081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999734-G-A

43884081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999734-G-T

43884082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999735-T-C

43884086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999739-G-A

43884086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999739-G-T

http://identifiers.org/hco/22/GRCh38#43884099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83999748-C-A

43884099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999748-C-G

43884099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999748-C-T

http://identifiers.org/hco/22/GRCh38#43884109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83999758-C-A

43884109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999758-C-T

http://identifiers.org/hco/22/GRCh38#43884120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83999760-C-A

43884120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999760-C-G

43884120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999760-C-T

http://identifiers.org/hco/22/GRCh38#43884185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83999799-C-A

43884185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999799-C-T

43884248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83999857-T-C

43884248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83999857-T-G

43884265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 83999874-G-A

43884306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: 83999915-G-A

http://identifiers.org/hco/22/GRCh38#43884307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83999916-C-A

43884307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: 83999916-C-T

43884348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83999951-G-A

43884348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83999951-G-T

http://identifiers.org/hco/22/GRCh38#43884371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83999977-C-A

43884371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999977-C-T

http://identifiers.org/hco/22/GRCh38#43884374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83999980-C-A

43884374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 83999980-C-T

43884397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000004-C-T

43884433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000037-G-A

43884433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000037-G-T

43884494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000114-G-A

43884494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000114-G-T

43884502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000124-C-G

43884522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000149-G-A

43884522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000149-G-T

43884548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000163-G-A

43884548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000163-G-T

43884645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000264-C-T

43884884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84000501-A-G

43886034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001635-G-A

43886154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001728-C-T

43886189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001761-G-A

43886189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001761-G-T

http://identifiers.org/hco/22/GRCh38#43886215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84001771-C-A

43886215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001771-C-T

43886218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001774-C-T

43886247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001775-C-T

43886256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84001784-T-C

43886331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 84001837-A-G

43886343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 84001849-A-G

43886410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: 84001916-C-T

43886432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: 84001938-C-T

http://identifiers.org/hco/22/GRCh38#43886534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84002042-C-A

43886534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002042-C-T

http://identifiers.org/hco/22/GRCh38#43886549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84002061-C-A

43886549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002061-C-G

43886583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002097-G-T

43886599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002109-G-A

43886599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002109-G-C

43886599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002109-G-T

43886706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002152-C-T

43886727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002173-C-T

43886768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002216-C-T

43887160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002494-C-G

43887382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002653-C-G

43887643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: synonymous variant
orthologous variants: 84002871-G-A

http://identifiers.org/hco/22/GRCh38#43887648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84002876-C-A

43887648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: missense variant
orthologous variants: 84002876-C-T

http://identifiers.org/hco/22/GRCh38#43887695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84002916-C-A

43887695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84002916-C-T

http://identifiers.org/hco/22/GRCh38#43887755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84002973-C-A

43887845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84003049-T-C

43887895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84003092-C-G

43889479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 84004534-G-A

43889596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004649-G-A

43889682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004723-A-G

http://identifiers.org/hco/22/GRCh38#43889707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84004748-A-C

43889707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004748-A-G

http://identifiers.org/hco/22/GRCh38#43889713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84004755-C-A

43889713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004755-C-T

43889720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004762-T-C

43889739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004781-C-G

43889739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004781-C-T

http://identifiers.org/hco/22/GRCh38#43889751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84004793-C-A

43889751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84004793-C-T

43890626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84006136-G-C

43890679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84006189-A-T

43890762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84006274-G-T

http://identifiers.org/hco/22/GRCh38#43891039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84006535-C-A

43891070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 84006564-G-A

43891070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 84006564-G-T

http://identifiers.org/hco/22/GRCh38#43891143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84006637-C-A

http://identifiers.org/hco/22/GRCh38#43891215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84006709-C-A

43891215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 84006709-C-G

43891215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 84006709-C-T

43891218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 84006712-G-A

43891218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 84006712-G-T

43891233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 84006727-G-C

43891233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 84006727-G-T

43891340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006843-T-C

43891340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006843-T-G

http://identifiers.org/hco/22/GRCh38#43891356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84006860-C-A

43891356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006860-C-G

43891356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006860-C-T

http://identifiers.org/hco/22/GRCh38#43891357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84006861-C-A

43891357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006861-C-T

43891389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006892-G-A

43891389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006892-G-T

43891414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84006914-T-C

43891647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84007089-G-A

43891647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: intron variant
orthologous variants: 84007089-G-T

http://identifiers.org/hco/22/GRCh38#43891692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84007126-C-A

43891692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007126-C-G

43891692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007126-C-T

43891712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 84007146-T-C

43891731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007165-A-G

http://identifiers.org/hco/22/GRCh38#43891734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84007168-C-A

43891734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007168-C-G

43891734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007168-C-T

43891773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007207-C-T

43891849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 84007283-T-C

43891875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007309-G-A

43891875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84007309-G-T

43891898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007319-G-A

43891898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007319-G-T

43891910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007331-C-G

43891910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007331-C-T

43891911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007332-G-C

43891911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007332-G-T

43891913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007334-G-A

43891913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007334-G-T

43891980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007395-G-A

43891980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007395-G-T

43891986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007398-T-A

43891986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24888
most severe consequence: 5 prime UTR variant
orthologous variants: 84007398-T-C