48997105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95897113-C-T

48997115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95897103-T-G

48997133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95897079-G-T

48997283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95896928-G-A

48997283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95896928-G-T

48997325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95896881-T-C

http://identifiers.org/hco/17/GRCh38#48997389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95896825-C-A

48997389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95896825-C-G

48997389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95896825-C-T

48997599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95896606-G-A

48997599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95896606-G-T

48997640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95896565-G-T

48997685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95896520-G-A

48997700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95896505-T-C

48997716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95896488-G-A

48997824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95896379-A-G

48997948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95896254-G-C

http://identifiers.org/hco/17/GRCh38#48997998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95896178-C-A

48997998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95896178-C-G

48998238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895951-G-T

48998279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895921-C-T

http://identifiers.org/hco/17/GRCh38#48998306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95895894-C-A

48998306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895894-C-T

48998526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895668-G-T

48998542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895652-C-T

48998702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895505-A-G

48998750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895471-T-C

48998774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895450-C-G

48998993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895226-A-G

48999021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895206-G-A

48999021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895206-G-C

48999021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895206-G-T

48999088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895128-T-A

48999088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895128-T-C

http://identifiers.org/hco/17/GRCh38#48999241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95895002-C-A

48999241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95895002-C-T

http://identifiers.org/hco/17/GRCh38#48999352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95894889-C-A

48999352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95894889-C-G

48999540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95894692-T-C

48999734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95894491-C-G

48999971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95894263-T-C

49000019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95894204-A-G

49000210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95894028-C-T

49000617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95893629-G-A

49000632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95893614-A-G

49000708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95893541-T-C

49001093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95893119-G-A

49001098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95893114-A-T

49001177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95893050-T-A

49001346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95892888-A-G

49001680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95892664-A-G

49001728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95892612-G-A

49002079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95892234-G-A

49002115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95892198-T-C

49002130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95892183-T-A

49002130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95892183-T-C

49002644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95891582-G-C

49002728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95891525-T-A

49003300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95890994-G-A

49003556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95890523-G-A

49003611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95890311-C-T

49003824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95890176-T-G

49004030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95889971-C-T

49004617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95889624-G-A

49004617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95889624-G-T

49004758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95889072-C-T

49004926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888902-C-G

49004931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888897-G-A

49004931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888897-G-T

http://identifiers.org/hco/17/GRCh38#49005060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95888789-A-C

49005121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888741-C-T

49005275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888572-T-G

49005325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888549-C-T

49005330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888544-C-T

49005352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888529-G-A

49005409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888491-A-G

49005437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888463-A-G

49005563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888355-T-C

49005993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887189-T-C

http://identifiers.org/hco/17/GRCh38#49006083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95887127-A-C

49006083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887127-A-G

49006190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887052-G-A

49006240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95886974-G-A

49006447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95886779-A-G

49006683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95886558-T-C

49007283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95885975-A-G

49007585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95885727-A-G

49008586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884767-T-C

49008701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884665-T-A

49008703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884663-T-C

49012400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95883487-A-G

49012406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95883480-G-C

http://identifiers.org/hco/17/GRCh38#49012423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95883465-C-A

49012423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95883465-C-T

49012432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95883455-T-C

http://identifiers.org/hco/17/GRCh38#49012452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95883435-C-A

49012452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95883435-C-T

http://identifiers.org/hco/17/GRCh38#49012604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95883308-C-A

49012641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95883275-C-T

49012674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95883238-G-A

49012674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95883238-G-T

49013093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95882862-G-T

49013201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882755-A-G

http://identifiers.org/hco/17/GRCh38#49013448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95882569-C-A

49013448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95882569-C-T

http://identifiers.org/hco/17/GRCh38#49013491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95882526-C-A

49013491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95882526-C-T

http://identifiers.org/hco/17/GRCh38#49013500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95882517-C-A

49013684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882359-T-C

49013769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882265-G-T

http://identifiers.org/hco/17/GRCh38#49013823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95882216-C-A

49013823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95882216-C-G

49013823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95882216-C-T

http://identifiers.org/hco/17/GRCh38#49013871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95882169-C-A

49013871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95882169-C-G

49013871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95882169-C-T

49013966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882088-C-G

49013966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882088-C-T

49013989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882068-A-G

49014002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882056-G-A

49014002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95882056-G-T

49014108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881975-G-A

49014219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881894-T-C

49015306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881288-G-T

49015322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881283-G-A

49015423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881206-C-T

49015579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881073-G-A

49015583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881069-T-G

49015783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95880839-T-C

49015874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95880697-C-T

49016182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95880403-G-A

49016363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95880217-A-G

49016426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95880001-T-C

49016651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879764-G-C

49016668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879747-T-A

49016674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879722-C-G

49016680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879716-C-G

49016758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879627-C-G

49016758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879627-C-T

49016902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879521-C-T

http://identifiers.org/hco/17/GRCh38#49016906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95879518-C-A

http://identifiers.org/hco/17/GRCh38#49016988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95879428-A-C

49017122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879308-A-G

49017231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95879205-A-G

49017299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95879144-C-T

49022339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873692-C-T

49022376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873661-A-G

49023774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871855-G-A

49023804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871824-A-G

49024470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871646-G-C

49024707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871398-A-G

49024902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871202-A-G

49025444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95870695-G-A

49025478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95870661-T-C

49025637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 95870474-C-T

49025747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95870369-A-G

http://identifiers.org/hco/17/GRCh38#49026295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95870293-C-A

49026295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95870293-C-T

49026338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95870249-A-G

49026524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95870100-G-C

49031985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95866073-G-A

http://identifiers.org/hco/17/GRCh38#49031989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95866069-A-C

49031989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95866069-A-G

49031989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95866069-A-T

49031994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95866064-G-A

49032145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95865982-G-C

49032147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95865980-G-A

49032147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95865980-G-T

49032213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95865947-A-G

49032354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95865842-G-A

49038151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95865057-T-C

49038244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95864968-G-A

49038439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, missense_variant
orthologous variants: 95864773-A-G

49038486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864734-T-A

49038486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864734-T-C

49038510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864715-A-T

49038551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864673-T-C

http://identifiers.org/hco/17/GRCh38#49038860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95864378-A-C

49039851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864095-A-G

http://identifiers.org/hco/17/GRCh38#49039856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95864090-C-A

49039856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864090-C-T

49039887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864059-G-A

http://identifiers.org/hco/17/GRCh38#49039905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95864055-A-C

49039905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95864055-A-G

49039982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, missense_variant
orthologous variants: 95863978-G-A

49041388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense variant
orthologous variants: 95861605-G-T

49041424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense variant
orthologous variants: 95861569-G-C

49041523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95861471-T-C

49041524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95861470-G-A

49041529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95861465-T-C

49041630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95861365-G-A

49041736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95861284-C-T

49041758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95861269-C-T

49042075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95860966-T-C

http://identifiers.org/hco/17/GRCh38#49042108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95860946-A-C

49042108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95860946-A-G

http://identifiers.org/hco/17/GRCh38#49042151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95860903-C-A

49042351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense variant
orthologous variants: 95860699-T-C

49042384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 95860666-G-A

49042384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 95860666-G-T

49042408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95860642-C-G

49042408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95860642-C-T

49043384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859784-C-G

49043384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859784-C-T

49043698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859554-T-C

49043750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859516-G-A

49043846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859435-G-A

49043846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859435-G-T

49043877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859405-T-A

49043877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859405-T-G

49043913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859368-T-C

49043913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859368-T-G

49043931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859340-T-G

49043957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859316-A-G

49044072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense variant
orthologous variants: 95859201-A-G

49044072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense variant
orthologous variants: 95859201-A-T

49044337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95859022-A-G

49044446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858915-G-A

49044652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858752-C-T

49044742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858660-G-C

49044857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858552-C-T

49044918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858516-G-A

http://identifiers.org/hco/17/GRCh38#49045087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95858351-C-A

49045087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858351-C-G

49045125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858310-C-T

http://identifiers.org/hco/17/GRCh38#49045172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95858263-C-A

49045172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858263-C-G

49045183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858252-T-A

49045183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858252-T-C

49045183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858252-T-G

49045206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95858229-A-G

49045854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857640-A-G

49045995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense variant
orthologous variants: 95857501-C-T

http://identifiers.org/hco/17/GRCh38#49046055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95857460-C-A

49046055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857460-C-T

http://identifiers.org/hco/17/GRCh38#49046125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95857402-C-A

49046125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857402-C-G

49046125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857402-C-T

http://identifiers.org/hco/17/GRCh38#49046167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95857352-C-A

49046167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857352-C-G

http://identifiers.org/hco/17/GRCh38#49046169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95857350-A-C

49046169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857350-A-G

49046169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857350-A-T

49046185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857328-T-C

http://identifiers.org/hco/17/GRCh38#49046199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95857314-C-A

49046199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857314-C-G

49046199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857314-C-T

http://identifiers.org/hco/17/GRCh38#49046207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95857219-C-A

49046207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95857219-C-T

49046341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: missense variant
orthologous variants: 95857033-G-A

49046425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95856952-G-A

http://identifiers.org/hco/17/GRCh38#49046472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95856907-C-A

49046474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95856901-T-A

49046474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95856901-T-C

49046474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95856901-T-G

49047086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: intron variant
orthologous variants: 95856126-C-G

49049951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853812-A-G

49049951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853812-A-T

49049968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853791-T-C

49050264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853396-A-G

49050277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853383-A-G

49050298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853365-T-C

http://identifiers.org/hco/17/GRCh38#49050481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95853186-C-A

http://identifiers.org/hco/17/GRCh38#49050506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95853169-A-C

49050506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853169-A-G

49050522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853150-T-C

49050558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95853113-T-C

http://identifiers.org/hco/17/GRCh38#49050575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95853096-C-A

49050748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95852921-G-A

http://identifiers.org/hco/17/GRCh38#49050767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95852902-A-C

49050863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95852808-C-T

49051448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95852241-G-A

49051532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95852197-G-A

49051532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95852197-G-T

49051541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95852188-G-T

49051579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95852176-G-T

http://identifiers.org/hco/17/GRCh38#49051618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95852139-C-A

49051915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851856-A-G

49051949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851825-T-C

49052016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851761-G-T

49052060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851715-G-T

49052065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851710-G-T

49052396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851438-G-A

49052419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851417-G-A

49052700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95851148-G-A

http://identifiers.org/hco/17/GRCh38#49053142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95850720-C-A

49053289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95850587-C-T

49053514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95850373-A-G

http://identifiers.org/hco/17/GRCh38#49053560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95850339-C-A

http://identifiers.org/hco/17/GRCh38#49053822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95850094-C-A

49053822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95850094-C-T

49053829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95850087-T-C

49053867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95850049-G-A

49053923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849991-A-G

49053923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849991-A-T

49054018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849909-A-G

49054034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849893-T-C

49054068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849854-G-A

49054079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849843-T-G

http://identifiers.org/hco/17/GRCh38#49054096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849826-C-A

49054096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849826-C-T

49054137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849792-T-C

http://identifiers.org/hco/17/GRCh38#49054162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849771-C-A

49054162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849771-C-T

49054177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849757-T-C

49054215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849741-G-A

49054215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849741-G-T

49054226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849728-T-G

49054337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849624-T-C

49054411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849550-C-T

49054471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849494-T-C

49054497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849469-G-A

49054497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849469-G-T

http://identifiers.org/hco/17/GRCh38#49054498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849468-C-A

49054498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849468-C-T

http://identifiers.org/hco/17/GRCh38#49054511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849454-C-A

49054511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849454-C-G

49054511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849454-C-T

49054602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849343-T-C

49054602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849343-T-G

49054604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849341-T-C

49054647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849300-A-G

http://identifiers.org/hco/17/GRCh38#49054659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849288-C-A

49054659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849288-C-T

49054676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849275-G-A

49054676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849275-G-T

49054685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849266-A-G

http://identifiers.org/hco/17/GRCh38#49054695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849256-C-A

49054695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849256-C-T

49054715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849236-A-G

49054778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849190-G-A

49054778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849190-G-T

http://identifiers.org/hco/17/GRCh38#49054784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849184-C-A

49054784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849184-C-T

49054828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849151-G-T

49054832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849147-G-T

http://identifiers.org/hco/17/GRCh38#49054833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849146-C-A

49054834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849145-T-C

49054841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849138-G-A

49054841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849138-G-T

49054858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95849111-G-A

http://identifiers.org/hco/17/GRCh38#49054959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95849020-A-C

49055126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848856-T-A

49055126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848856-T-G

49055166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848815-A-T

http://identifiers.org/hco/17/GRCh38#49055167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95848814-A-C

49055167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848814-A-G

49055167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848814-A-T

49055168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848813-A-T

49055274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848710-A-T

49055312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848693-A-T

49055329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848676-C-T

49055360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848649-T-A

49055360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848649-T-C

49055361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848648-A-G

49055499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848554-T-C

49055614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848469-G-A

49055614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848469-G-T

http://identifiers.org/hco/17/GRCh38#49055689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95848393-C-A

49055796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848297-G-A

49055884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848244-A-T

49055890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848238-G-A

49055890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848238-G-T

49055941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848187-G-A

49056061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28866
most severe consequence: 3 prime UTR variant
orthologous variants: 95848068-T-C