http://identifiers.org/hco/17/GRCh38#6393702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71902617-A-C

6393702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: missense variant
orthologous variants: 71902617-A-T

6393709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: missense variant
orthologous variants: 71902624-G-A

6393709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: missense variant
orthologous variants: 71902624-G-T

6393759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: missense variant
orthologous variants: 71902669-G-A

6393759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: missense variant
orthologous variants: 71902669-G-C

6393766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: missense variant
orthologous variants: 71902676-T-C

6394000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71902705-G-A

6394069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71902765-C-T

6394553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903235-C-T

6394685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903368-C-T

6394707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903390-T-C

6394959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903565-G-A

6394959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903565-G-C

6395238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903760-G-A

6395239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903761-C-T

6395291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903810-G-A

6395297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903816-A-G

http://identifiers.org/hco/17/GRCh38#6395335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71903850-C-A

6395335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71903850-C-T

6401093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71907703-G-C

6401095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71907705-G-A

6401114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71907726-G-A

6401114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71907726-G-C

6401154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71907771-T-A

6401305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71907900-G-A

6401436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71908011-A-G

6401513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71908087-C-T

6401543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71908121-G-T

6401551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71908129-T-A

6401551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71908129-T-G

6401712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71908286-A-T

6401777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71908351-T-C

http://identifiers.org/hco/17/GRCh38#6402617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71908918-C-A

6402709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909015-A-G

6402805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909106-G-T

6403278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909449-C-G

6403278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909449-C-T

http://identifiers.org/hco/17/GRCh38#6403280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71909451-A-C

6403287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909454-G-T

6403325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909472-T-C

http://identifiers.org/hco/17/GRCh38#6403440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71909523-C-A

6403440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909523-C-T

6403496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909576-C-G

6403553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909624-C-G

6403591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909662-T-C

6403591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909662-T-G

6403740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71909805-A-G

6403802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71910420-T-C

6404030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71910660-T-C

6404057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71910687-A-G

http://identifiers.org/hco/17/GRCh38#6404067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71910697-A-C

6404067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71910697-A-G

http://identifiers.org/hco/17/GRCh38#6404202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71910822-C-A

6404397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71911052-G-T

6404462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71911183-A-T

6404525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71911523-C-T

6405639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71911918-A-G

6405665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71911972-G-A

6405665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71911972-G-T

6405672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71911979-A-G

http://identifiers.org/hco/17/GRCh38#6405928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71912326-C-A

6405928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912326-C-T

6408561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912787-C-G

6408563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912789-G-A

6408569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912795-G-A

6408689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912932-G-A

6408689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912932-G-T

6408718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912961-A-G

6408752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912998-G-A

6408752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71912998-G-T

6408889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71913134-G-A

6409034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71913265-G-A

6409053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71913274-A-G

6409153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71913351-T-C

6409853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71914342-A-G

http://identifiers.org/hco/17/GRCh38#6409870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71914359-C-A

6410320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71914501-C-G

6410365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71914545-T-A

6412716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71915013-C-T

6413249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71915481-T-A

6413347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71915563-A-G

6413559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71915742-C-T

6413690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71915862-T-C

6413691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71915863-G-A

6417405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71917666-T-C

http://identifiers.org/hco/17/GRCh38#6417540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71917781-C-A

6422797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71918316-G-C

6422803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71918322-G-A

http://identifiers.org/hco/17/GRCh38#6422805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71918324-A-C

6422814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71918333-T-G

6422825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71918344-C-T

http://identifiers.org/hco/17/GRCh38#6422984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71918485-C-A

http://identifiers.org/hco/17/GRCh38#6423025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71918514-C-A

6423025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71918514-C-T

6423059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: intron variant
orthologous variants: 71918546-T-C

6423871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71918916-G-T

6425387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71919830-G-A

6425387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71919830-G-T

6425412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71919855-G-T

6425439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71919880-T-C

6425676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71920128-C-G

6425676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71920128-C-T

6425775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71920227-C-G

6425775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71920227-C-T

6425836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 71920288-G-A

6425836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 71920288-G-T

6425856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920298-T-C

6425930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920332-G-A

6425930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920332-G-T

6426019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920353-C-G

6426064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920397-G-T

http://identifiers.org/hco/17/GRCh38#6426089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71920418-C-A

http://identifiers.org/hco/17/GRCh38#6426170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71920497-A-C

http://identifiers.org/hco/17/GRCh38#6426173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71920500-A-C

6426189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920516-G-A

6426350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920629-G-T

6426371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920711-A-G

6426401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920792-T-C

6426401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920792-T-G

http://identifiers.org/hco/17/GRCh38#6426410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71920801-C-A

6426410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920801-C-T

6426463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920857-T-A

http://identifiers.org/hco/17/GRCh38#6426471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71920865-C-A

6426471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920865-C-T

6426485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920879-C-T

6426556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920965-T-A

6426556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71920965-T-G

6426643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71921061-G-A

6426658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71921076-A-G

http://identifiers.org/hco/17/GRCh38#6426760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71921178-C-A

6426760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 71921178-C-T

6426941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71921312-G-A

6426941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 71921312-G-C

6426947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71921318-G-A

6426977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71921348-G-A

6426977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71921348-G-T

http://identifiers.org/hco/17/GRCh38#6426992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71921363-C-A

6426992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71921363-C-T

6426993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71921364-G-A

6427122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71921496-G-A

6427204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71921589-G-A

6427204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71921589-G-T

6427374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71921763-C-T

http://identifiers.org/hco/17/GRCh38#6427428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71921810-C-A

6427687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71921950-C-T

http://identifiers.org/hco/17/GRCh38#6428174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71922124-C-A

6428174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922124-C-T

6428184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922134-T-C

6428184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922134-T-G

6428232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922174-G-A

6428232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922174-G-T

http://identifiers.org/hco/17/GRCh38#6428235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71922177-C-A

6428235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922177-C-G

6428235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922177-C-T

6428290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922221-C-T

6428327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71922252-C-T

http://identifiers.org/hco/17/GRCh38#6428390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71922315-C-A

6428390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71922315-C-G

6428390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71922315-C-T

6428420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71922345-G-A

6428420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 71922345-G-T

http://identifiers.org/hco/17/GRCh38#6428423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71922348-C-A

6428423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71922348-C-T

6428450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71922375-C-T

6428459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71922384-G-T

http://identifiers.org/hco/17/GRCh38#6428520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71922445-C-A

6428520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922445-C-T

6428525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922450-G-A

6428525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922450-G-T

6428533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922455-T-A

6428600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922514-A-T

6428644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922557-G-A

6428644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922557-G-T

6428648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922561-G-T

6428906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71922816-C-T

6429344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923024-T-C

6429356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923036-T-C

6429954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924693-G-A

6430017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924771-T-C

6430555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924914-G-A

6430620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924963-A-T

6430638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924981-T-G

6430872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71925234-A-G

6430969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71925329-C-T

6431268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71925488-G-A

6431560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71925604-C-T

http://identifiers.org/hco/17/GRCh38#6433819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71927354-C-A

6433819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71927354-C-T

http://identifiers.org/hco/17/GRCh38#6433847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71927381-C-A

6433847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71927381-C-T

6433906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71927425-A-G

6433912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 71927431-T-A

6433912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 71927431-T-C

6433912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 71927431-T-G

http://identifiers.org/hco/17/GRCh38#6434187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71927709-C-A

http://identifiers.org/hco/17/GRCh38#6434225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71927750-C-A

6434348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71927862-C-G

http://identifiers.org/hco/17/GRCh38#6434733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71927929-A-C

6434744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71927939-A-G

http://identifiers.org/hco/17/GRCh38#6434868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71928072-A-C

6434868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71928072-A-G

6434969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71928157-C-T

6434994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71928176-A-G

6434994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71928176-A-T

6435011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 71928191-G-A

6435012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71928192-G-C

6435112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71928291-G-A

http://identifiers.org/hco/17/GRCh38#6435118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71928297-A-C

6435118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71928297-A-G

6435157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5 prime UTR variant
orthologous variants: 71928396-G-A

6435157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5 prime UTR variant
orthologous variants: 71928396-G-C

http://identifiers.org/hco/17/GRCh38#6435179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71928416-A-C

http://identifiers.org/hco/17/GRCh38#6435193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71928430-A-C

6435193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5 prime UTR variant
orthologous variants: 71928430-A-G

http://identifiers.org/hco/17/GRCh38#6435196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 359
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71928433-C-A