94394960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4505768-C-T

http://identifiers.org/hco/7/GRCh38#94395160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4505968-C-A

94395160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4505968-C-T

94395185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4505995-A-G

http://identifiers.org/hco/7/GRCh38#94395216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4506028-C-A

94395216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4506028-C-T

http://identifiers.org/hco/7/GRCh38#94395220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4506032-C-A

http://identifiers.org/hco/7/GRCh38#94395221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4506033-A-C

94395221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4506033-A-G

http://identifiers.org/hco/7/GRCh38#94395357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4506159-C-A

94395390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4506192-T-C

http://identifiers.org/hco/7/GRCh38#94395458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4506254-C-A

94395472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4506268-T-C

94395520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4506316-C-T

94395708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4506486-T-C

http://identifiers.org/hco/7/GRCh38#94395758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4506528-C-A

94395760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4506530-G-T

http://identifiers.org/hco/7/GRCh38#94395776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4506546-A-C

94396019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4506766-C-T

94396275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4507020-G-T

94396898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4507575-T-G

94396963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4507640-A-G

94397047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4507715-T-A

94397047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4507715-T-C

http://identifiers.org/hco/7/GRCh38#94397380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4507944-C-A

94397600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508169-T-C

94397727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508317-T-C

94397727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508317-T-G

94397761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508348-G-A

94397761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508348-G-T

94397792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508384-A-G

http://identifiers.org/hco/7/GRCh38#94397857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4508431-C-A

94397857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508431-C-T

94398129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508700-G-C

94398164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508729-C-T

94398206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508768-T-G

94398263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508821-T-A

94398299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508857-G-A

94398299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508857-G-T

94398320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508877-G-T

94398358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508916-A-G

94398393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4508951-A-G

94398433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4508990-T-C

http://identifiers.org/hco/7/GRCh38#94398978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4509537-A-C

94399000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4509559-A-G

94399126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4509683-G-T

94399181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4509739-T-C

94399787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510313-T-C

94399997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510468-C-T

94400062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510536-A-G

94400062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510536-A-T

94400063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510537-T-C

http://identifiers.org/hco/7/GRCh38#94400212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4510700-C-A

94400212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense variant
orthologous variants: 4510700-C-G

94400212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense variant
orthologous variants: 4510700-C-T

94400280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense variant
orthologous variants: 4510786-C-T

94400349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510870-G-A

94400349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510870-G-T

94400425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510946-T-C

94400479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4510998-G-T

94400592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4511111-G-A

94401040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4511557-A-G

94401325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4511825-G-C

94401471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512219-A-G

94401529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512313-T-A

94401529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512313-T-C

http://identifiers.org/hco/7/GRCh38#94401531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4512315-A-C

94401531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512315-A-G

94401531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512315-A-T

94401544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512336-A-G

94401544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512336-A-T

94401635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512431-T-C

94401637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512433-A-G

94401673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512469-T-C

94401722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512506-T-A

94401722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512506-T-C

94401751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512535-T-C

94401807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512598-A-G

94402001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512743-G-A

94402199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4512902-A-G

http://identifiers.org/hco/7/GRCh38#94402469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4513149-A-C

94402473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4513153-T-C

94402596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4513266-C-T

94402622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4513292-A-G

94403005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4513657-T-C

94403280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4513944-C-G

94403329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4513993-G-A

http://identifiers.org/hco/7/GRCh38#94403469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4514116-C-A

94403773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4514424-G-A

94404126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4514789-T-C

94404300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4514950-T-A

94404300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4514950-T-C

http://identifiers.org/hco/7/GRCh38#94404456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4515112-A-C

http://identifiers.org/hco/7/GRCh38#94404501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4515161-C-A

http://identifiers.org/hco/7/GRCh38#94404504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4515164-C-A

94404642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4515294-A-G

94404725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4515513-G-A

94404794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4515586-T-C

94405101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4515895-T-C

94405101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4515895-T-G

94405107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4515900-A-G

94405108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4515901-A-T

94405193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4515955-G-A

94405276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4516038-T-C

http://identifiers.org/hco/7/GRCh38#94405354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4516094-C-A

94405496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4516229-C-T

http://identifiers.org/hco/7/GRCh38#94405529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4516261-A-C

94405529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4516261-A-G

94405529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4516261-A-T

http://identifiers.org/hco/7/GRCh38#94405733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4516452-A-C

94405733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4516452-A-G

94405787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4516513-G-C

94405793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4516519-T-A

94406375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4517020-T-G

94406508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4517145-A-G

94406635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4517269-G-A

94406763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4517397-A-G

94406969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4517603-G-A

94407116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4517757-C-T

94407410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518020-T-C

94407414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518024-T-C

94407469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518078-C-T

94407667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518279-A-G

94407667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518279-A-T

94407734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518345-A-G

http://identifiers.org/hco/7/GRCh38#94407825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4518447-A-C

94407825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518447-A-T

94408190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense variant
orthologous variants: 4518798-G-A

94408190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense variant
orthologous variants: 4518798-G-T

http://identifiers.org/hco/7/GRCh38#94408295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4518906-A-C

94408295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518906-A-G

94408304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518914-T-G

94408307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4518917-A-T

94408833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4519356-C-T

94408883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4519403-A-G

94408883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4519403-A-T

94408975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4519489-C-T

94409031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4519529-A-G

94409182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4519700-A-T

http://identifiers.org/hco/7/GRCh38#94409194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4519715-A-C

94409431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4519939-A-G

http://identifiers.org/hco/7/GRCh38#94409527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4520003-A-C

94409527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520003-A-G

94409538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520014-T-C

94409538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520014-T-G

http://identifiers.org/hco/7/GRCh38#94409575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4520049-A-C

http://identifiers.org/hco/7/GRCh38#94409715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4520161-C-A

94409717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4520165-T-C

94409743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4520191-G-A

94409743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4520191-G-C

http://identifiers.org/hco/7/GRCh38#94409761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4520209-A-C

94409761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4520209-A-T

94409779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4520227-C-T

94409876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520294-T-C

94409906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520324-T-C

94409976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520403-C-G

94409976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520403-C-T

94410220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520575-A-G

94410342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4520699-C-T

http://identifiers.org/hco/7/GRCh38#94410417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4520769-C-A

94410417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4520769-C-T

94410788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521127-G-A

94410788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521127-G-T

94410862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521203-C-G

94410862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521203-C-T

94411029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521372-A-G

94411029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521372-A-T

94411040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521383-T-A

94411040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521383-T-G

http://identifiers.org/hco/7/GRCh38#94411124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4521464-C-A

94411217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521557-G-T

94411274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521615-G-A

94411274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521615-G-T

94411424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521770-C-T

94411535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521881-C-T

94411651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521995-G-A

94411651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4521995-G-C

94411712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4522059-A-G

94411954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4522331-A-G

94411975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4522349-G-C

94412483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4522857-G-T

94412517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4522892-G-A

94412655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4523027-T-C

94412670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: synonymous variant
orthologous variants: 4523042-C-G

94412809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523209-G-A

94412809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523209-G-C

94412809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523209-G-T

94412904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523294-C-T

94413052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523445-T-A

94413078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4523589-T-C

94413078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4523589-T-G

94413088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense variant
orthologous variants: 4523599-T-A

94413147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523658-A-G

94413151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523660-G-T

94413162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523671-T-A

94413162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523671-T-C

94413162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523671-T-G

http://identifiers.org/hco/7/GRCh38#94413257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4523744-C-A

94413299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523790-A-G

94413459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron variant
orthologous variants: 4523947-A-T

94413842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4524405-C-T

http://identifiers.org/hco/7/GRCh38#94414088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4524751-C-A

94414095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4524758-G-T

http://identifiers.org/hco/7/GRCh38#94414144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4524800-C-A

94414144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4524800-C-T

http://identifiers.org/hco/7/GRCh38#94414172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4524828-C-A

94414172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4524828-C-G

http://identifiers.org/hco/7/GRCh38#94414208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4524864-C-A

94414208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4524864-C-G

94414208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4524864-C-T

http://identifiers.org/hco/7/GRCh38#94414243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4524897-C-A

94414243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4524897-C-G

94414379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4525024-G-A

94414379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4525024-G-T

http://identifiers.org/hco/7/GRCh38#94414579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4525226-C-A

94414579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4525226-C-T

94414731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4525382-G-T

94414821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4525472-A-G

94415119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4525768-T-C

94415291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4525947-T-C

94415375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526028-G-A

94415375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526028-G-T

http://identifiers.org/hco/7/GRCh38#94415412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4526049-A-C

94415412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526049-A-G

94415412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526049-A-T

94415423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526060-T-C

94415423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526060-T-G

94415535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526175-A-G

94415673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526310-A-T

94415712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526346-T-C

94415894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526558-A-T

94415922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526586-A-G

94416176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526846-C-T

94416240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526911-A-G

http://identifiers.org/hco/7/GRCh38#94416292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4526966-C-A

94416292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526966-C-T

94416317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4526993-A-G

94416335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527009-C-G

94416335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527009-C-T

94416524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527172-T-C

94416531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527179-G-A

94416531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527179-G-T

94416568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527212-A-G

94416568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527212-A-T

94416618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527263-G-T

http://identifiers.org/hco/7/GRCh38#94416682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4527318-A-C

94416682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527318-A-G

94416744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527373-G-A

94416744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527373-G-T

94416792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4527418-A-G

94417111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527705-G-A

94417131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527725-A-G

94417195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527787-G-A

94417216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527808-C-G

94417351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527935-G-C

94417351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527935-G-T

94417402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527985-T-G

94417416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4527999-T-C

http://identifiers.org/hco/7/GRCh38#94417521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4528106-C-A

94417521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4528106-C-T

94417667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4528246-G-T

94417745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4528327-G-A

94417745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4528327-G-T

94417835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528423-C-T

94417836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528424-G-A

94417836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528424-G-C

94417836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528424-G-T

http://identifiers.org/hco/7/GRCh38#94417843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4528431-C-A

94417843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528431-C-T

http://identifiers.org/hco/7/GRCh38#94417844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4528432-C-A

94417844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528432-C-T

94417884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528472-G-A

http://identifiers.org/hco/7/GRCh38#94417887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4528475-C-A

94417887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528475-C-G

94417887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528475-C-T

94417888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528476-A-G

94417958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528542-T-G

94418140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528723-A-T

94418170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528753-G-A

94418182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528765-G-A

94418192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528775-A-G

94418297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528873-G-C

94418350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528926-A-G

94418350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4528926-A-T

94418446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529015-G-A

94418446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529015-G-T

94418688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529269-G-T

94418915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529473-G-A

94418987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529538-A-G

94419290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529791-C-G

94419321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529811-T-G

94419331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529821-T-A

94419331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529821-T-C

94419365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529855-G-T

http://identifiers.org/hco/7/GRCh38#94419366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4529856-C-A

94419366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529856-C-T

94419381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4529989-A-G

94419391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530010-A-G

94419417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530078-G-A

94419417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530078-G-T

94419463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4530134-G-T

94419479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4530150-G-A

94419479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4530150-G-C

94419492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4530164-T-A

94419559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4530233-T-C

94419561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530235-C-T

94419647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530356-T-C

http://identifiers.org/hco/7/GRCh38#94419654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4530363-C-A

94419654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530363-C-G

94419677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530402-A-G

94420142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530858-T-C

94420208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4530925-A-G

94420328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4531051-A-G

94420766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4531453-T-C

http://identifiers.org/hco/7/GRCh38#94420940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4531821-C-A

94420980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4531865-T-C

94420980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4531865-T-G

94421003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4531889-A-G

http://identifiers.org/hco/7/GRCh38#94421108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4531986-C-A

http://identifiers.org/hco/7/GRCh38#94421110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4531988-A-C

94421110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4531988-A-G

94421145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532023-A-G

94421210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532124-T-A

94421241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532155-T-C

94421241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532155-T-G

94421242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532156-G-T

94421285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532206-C-G

94421285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532206-C-T

94421303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532224-A-G

94421303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4532224-A-T

94421441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4532322-C-T

94421476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4532357-G-C

94421476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4532357-G-T

http://identifiers.org/hco/7/GRCh38#94421501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4532381-A-C

94421678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4532536-A-G

94421694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4532552-G-T

94421695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4532553-T-C

94421777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4532629-C-T

94422157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4533004-T-A

94422157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4533004-T-C

94422461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4533294-T-G

http://identifiers.org/hco/7/GRCh38#94422555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4533389-C-A

94422555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4533389-C-T

94422572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4533406-T-A

94422610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4533442-T-A

94422732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4533558-G-A

94422732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4533558-G-T

94422836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4533621-G-A

94422836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4533621-G-T

http://identifiers.org/hco/7/GRCh38#94423265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4534049-C-A

94423265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534049-C-T

94423335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534120-T-A

http://identifiers.org/hco/7/GRCh38#94423336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4534121-C-A

94423343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534128-A-T

http://identifiers.org/hco/7/GRCh38#94423350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4534136-A-C

http://identifiers.org/hco/7/GRCh38#94423353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4534139-C-A

94423353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534139-C-T

94423365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534151-T-G

94423408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534184-G-T

94423456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534231-T-G

94423468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534243-C-T

94423517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534292-G-A

94424045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534324-G-C

94424141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534386-G-A

94424141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534386-G-C

94424141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4534386-G-T

94424285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4534529-G-A

94424285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4534529-G-C

94424595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4534840-G-C

94424637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4534882-A-G

http://identifiers.org/hco/7/GRCh38#94424674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4534918-C-A

94424674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4534918-C-T

http://identifiers.org/hco/7/GRCh38#94424678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4534922-C-A

94424678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4534922-C-T

94424696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4534940-T-A

94424696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4534940-T-C

94424696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4534940-T-G

94424767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535017-T-A

94424782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535033-G-A

94424782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535033-G-C

94424782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535033-G-T

94424844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535093-A-G

94424927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535190-T-C

94424933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535196-T-C

94425046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535309-T-A

94425046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535309-T-C

94425046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535309-T-G

94425389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535639-A-G

94425601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4535822-T-G

http://identifiers.org/hco/7/GRCh38#94425624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4535845-C-A

94425624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4535845-C-T

94425698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4535920-G-A

94425899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536112-G-A

94425899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536112-G-C

http://identifiers.org/hco/7/GRCh38#94425922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4536131-C-A

94425922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536131-C-T

94425972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536182-T-A

94426121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536325-G-T

94426199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536393-G-C

http://identifiers.org/hco/7/GRCh38#94426202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4536396-C-A

94426202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536396-C-G

94426202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536396-C-T

http://identifiers.org/hco/7/GRCh38#94426307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4536484-C-A

94426307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536484-C-G

94426339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4536516-A-G

94426455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4536629-G-A

http://identifiers.org/hco/7/GRCh38#94426546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4536720-C-A

94426546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4536720-C-T

94426664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4536821-A-G

http://identifiers.org/hco/7/GRCh38#94426812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4536970-C-A

94426812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4536970-C-T

94426870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4537029-G-T

94426918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4537078-T-A

94426918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4537078-T-C

94426971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4537130-G-A

http://identifiers.org/hco/7/GRCh38#94427084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4537246-A-C

94427084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4537246-A-G

94427121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4537284-G-A

94427127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4537290-G-A

94427127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4537290-G-C

94427127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4537290-G-T

94427166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4537328-A-G

94427166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4537328-A-T

94427327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537489-A-G

94427334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537496-A-T

94427399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537560-T-G

94427492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537644-A-G

94427492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537644-A-T

94427509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537661-T-G

http://identifiers.org/hco/7/GRCh38#94427528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4537680-C-A

94427528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537680-C-T

94427530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537682-T-C

94427540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4537692-T-C

94427633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4537784-C-G

94427633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4537784-C-T

http://identifiers.org/hco/7/GRCh38#94427731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4537882-A-C

94427731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4537882-A-G

94427779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4537930-G-A

94427779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4537930-G-T

94427782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4537933-T-C

94427794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4537945-G-A

94427794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4537945-G-C

94427794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4537945-G-T

94427875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4538026-G-A

94427954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538103-G-A

94427954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538103-G-T

http://identifiers.org/hco/7/GRCh38#94428008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4538161-C-A

94428008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538161-C-T

http://identifiers.org/hco/7/GRCh38#94428009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4538162-C-A

http://identifiers.org/hco/7/GRCh38#94428098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4538423-C-A

94428217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538554-C-G

94428482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538815-G-A

http://identifiers.org/hco/7/GRCh38#94428500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4538833-C-A

94428500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538833-C-G

94428500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538833-C-T

http://identifiers.org/hco/7/GRCh38#94428516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4538849-A-C

94428516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4538849-A-G

94428999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4539315-G-A

94429072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4539369-G-T

http://identifiers.org/hco/7/GRCh38#94429148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4539428-C-A

94429148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4539428-C-G

94429148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4539428-C-T

94429199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4539474-T-C

94429543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4539797-G-A

94429543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4539797-G-C

94429543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4539797-G-T

http://identifiers.org/hco/7/GRCh38#94429667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4539892-C-A

94429667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4539892-C-T

94429739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4539982-T-C

http://identifiers.org/hco/7/GRCh38#94429923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4540160-C-A

94429923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540160-C-T

94430004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540291-T-A

94430004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540291-T-C

94430066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540322-G-T

94430084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540342-A-G

94430084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540342-A-T

http://identifiers.org/hco/7/GRCh38#94430087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4540345-C-A

94430110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540367-A-G

http://identifiers.org/hco/7/GRCh38#94430115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4540372-C-A

94430115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540372-C-G

94430116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540373-T-G

94430131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540388-A-T

94430146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540405-G-T

http://identifiers.org/hco/7/GRCh38#94430155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4540414-C-A

94430161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540420-G-T

94430164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540423-G-A

94430164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540423-G-T

94430176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540435-T-C

94430190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540449-A-G

http://identifiers.org/hco/7/GRCh38#94430201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4540461-C-A

94430201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540461-C-T

94430209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4540469-G-T

94430349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4540618-G-A

http://identifiers.org/hco/7/GRCh38#94430405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4540674-C-A

94430604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4540885-T-A

94430604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4540885-T-G

http://identifiers.org/hco/7/GRCh38#94430803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4541109-C-A

94430982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: 3 prime UTR variant
orthologous variants: 4541284-A-T

94431188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2198
most severe consequence: 3 prime UTR variant
orthologous variants: 4541496-G-A