http://identifiers.org/hco/8/GRCh38#6708657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#18896564-C-A

6708657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 18896564-C-G

6708657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 18896564-C-T

6708662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5 prime UTR variant
orthologous variants: 18896569-T-C

6708662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5 prime UTR variant
orthologous variants: 18896569-T-G

6708778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 18896685-T-C

6708884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 18896791-C-G

6708884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 18896791-C-T

http://identifiers.org/hco/8/GRCh38#6708991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#18896871-C-A

6708991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 18896871-C-T

http://identifiers.org/hco/8/GRCh38#6709016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#18896892-C-A

6709016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 18896892-C-T

6709135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18897006-T-C

http://identifiers.org/hco/8/GRCh38#6709257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18897083-A-C

http://identifiers.org/hco/8/GRCh38#6709531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18897398-C-A

6709715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18897518-T-C

6709765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18897554-T-C

6709786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18897567-C-T

6713285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901200-A-G

6713285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901200-A-T

6713375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901284-C-T

6714001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901713-C-G

6714001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901713-C-T

http://identifiers.org/hco/8/GRCh38#6714099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18901799-C-A

6714099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901799-C-G

6714099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901799-C-T

6714268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901956-C-G

6714268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901956-C-T

6714288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18901974-T-A

6714411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18902078-A-G

6714633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903432-C-T

6714672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903472-C-T

6714686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903486-C-G

http://identifiers.org/hco/8/GRCh38#6714688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18903488-A-C

6714688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903488-A-G

6714960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903593-G-A

6715005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903640-G-T

6715030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903664-A-T

6715041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903674-C-T

6715085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903727-C-G

6715099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903741-G-A

6715126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903759-A-G

6715262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903887-G-T

6715349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18903972-G-A

6715528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904316-C-T

6715556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904344-C-T

6715582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904367-G-A

6715678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904450-C-T

6715712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904484-A-G

6715749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904526-A-G

6715843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904588-G-A

6715934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904691-G-A

6715939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904696-G-A

6715939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904696-G-C

6715939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904696-G-T

6716095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18904891-T-C

6716927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18905078-C-T

6716935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18905086-A-G

6717059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18905165-C-T

6717219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18905320-T-G

6717613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18905630-A-G

6717625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18905703-C-G

6717809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18905958-C-T

http://identifiers.org/hco/8/GRCh38#6717824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18905973-A-C

6717989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18906280-C-T

6718011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18906289-C-G

http://identifiers.org/hco/8/GRCh38#6721377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18907651-C-A

http://identifiers.org/hco/8/GRCh38#6721514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18907837-A-C

6721524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18907847-C-G

6721695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18908014-C-T

6722115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18908257-G-A

6722115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18908257-G-C

6722187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18908324-C-G

6722202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18908340-A-G

6722444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18908565-A-G

6723545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18910332-A-G

6723868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18910640-A-G

6724197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18910912-G-C

6724222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18910940-A-G

6724495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911166-C-T

6724605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911239-C-T

http://identifiers.org/hco/8/GRCh38#6724776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18911409-C-A

6724776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911409-C-T

6724960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911582-A-G

6724960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911582-A-T

6724969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911591-T-A

6724969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911591-T-C

6724969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18911591-T-G

6725637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913145-A-G

6725685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913191-T-C

6725899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913363-C-T

6725927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913414-A-G

6725974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913457-T-G

6726044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913504-G-C

6726083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913543-A-G

6726211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913651-A-G

6726212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913652-T-C

6726212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913652-T-G

6726233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18913667-C-T

6726683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914021-A-G

6726803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914207-C-G

6726865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914293-T-G

6726873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914301-G-A

6726873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914301-G-C

6727026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914463-G-C

6727027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914464-G-T

6727148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914556-T-C

6727148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914556-T-G

6727169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914577-C-G

6727212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914598-C-G

6727807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914795-C-T

6727812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914799-G-A

6727812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18914799-G-T

6728070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915027-G-A

6728260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915201-G-C

6728260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915201-G-T

6728296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915238-T-C

6728461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915517-C-G

6728471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915527-C-G

6728481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915537-G-C

6728640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18915688-T-A

http://identifiers.org/hco/8/GRCh38#6729028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18916116-A-C

6729028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18916116-A-G

6729365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18916534-T-G

6729368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18916537-C-T

6729559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18916688-T-C

6729863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18917631-G-A

6729907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18917679-A-G

6729947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18917719-G-C

6730009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18917978-G-T

6730073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18918035-G-A

6730114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18918089-T-C

6730135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18918110-G-C

6730167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18918133-G-A

http://identifiers.org/hco/8/GRCh38#6730742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18918940-C-A

6730742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, stop_gained
orthologous variants: 18918940-C-G

6730757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_lost, synonymous_variant
orthologous variants: 18918955-A-G

6730757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_lost, synonymous_variant
orthologous variants: 18918955-A-T

http://identifiers.org/hco/8/GRCh38#6730831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18919029-C-A

6730831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18919029-C-G

6730837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18919035-T-A

6730837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18919035-T-C

6730837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18919035-T-G

6732430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920725-T-C

6732439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920734-G-T

6732478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920774-G-A

6732478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920774-G-T

http://identifiers.org/hco/8/GRCh38#6732509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18920802-C-A

6732509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920802-C-G

6732509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920802-C-T

6732650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 18920943-A-G

6732665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920956-G-A

6732728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920999-T-A

6732728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18920999-T-G

6732768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921044-A-G

6732772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921048-T-G

6733105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921346-A-G

6733143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921382-G-C

6733143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921382-G-T

6733185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921427-G-C

6733201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921443-C-T

6733351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921536-C-T

6733366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18921551-C-T

http://identifiers.org/hco/8/GRCh38#6739910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18922240-C-A

http://identifiers.org/hco/8/GRCh38#6740020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18922331-A-C

6740031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922342-A-G

6740113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922428-C-G

6740133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922448-C-G

6740245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922556-A-G

6740314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922624-G-C

6740314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922624-G-T

6740316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922626-G-C

6740328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18922638-T-C

http://identifiers.org/hco/8/GRCh38#6740916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18925278-C-A

6740916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18925278-C-T

6741036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18925404-T-A

6741444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18925844-G-A

6741447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18925847-G-A

http://identifiers.org/hco/8/GRCh38#6741637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18926033-C-A

6741637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18926033-C-T

http://identifiers.org/hco/8/GRCh38#6741818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18926221-C-A

6741818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18926221-C-T

6741821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18926224-G-T

http://identifiers.org/hco/8/GRCh38#6741883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18926262-A-C

6741883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18926262-A-G

6746859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927632-A-G

6746882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927658-T-C

6747433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18927816-A-G

6747470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927853-A-G

6747497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927876-A-G

6747553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927917-G-A

6747553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927917-G-C

6747553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927917-G-T

6747568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927936-G-A

6747568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927936-G-C

6747568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927936-G-T

6747611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927974-A-G

6747611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927974-A-T

6747642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927991-T-A

6747642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18927991-T-C

6747812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18928168-G-C

6754985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18929553-T-G

6755014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18929586-A-G

6755019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18929591-A-G

6755024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18929596-A-G

6755186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18929756-C-T

6755190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18929760-T-A

http://identifiers.org/hco/8/GRCh38#6755292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18930068-C-A

6755292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18930068-C-G

6755292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18930068-C-T

6755347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18930123-G-A

6755392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18930156-G-C

6756099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18930533-T-A

6756135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18930546-G-C

6756135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18930546-G-T

6757028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931608-G-A

6757028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931608-G-T

6757065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931645-G-A

6757065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931645-G-T

6757088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931665-A-T

6757128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931708-G-A

6757128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931708-G-C

6757128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18931708-G-T

6757268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18931859-G-A

http://identifiers.org/hco/8/GRCh38#6757292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18931883-A-C

6757292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18931883-A-G

6757325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18931916-G-A

6757325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18931916-G-C

6757448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 18932024-A-G

6757654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932268-G-A

6757654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932268-G-T

6757717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932325-T-C

6757838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932454-A-T

6757933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932546-G-T

6758276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932848-T-C

http://identifiers.org/hco/8/GRCh38#6758312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18932880-A-C

6758317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932885-G-A

http://identifiers.org/hco/8/GRCh38#6758336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18932904-C-A

6758336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18932904-C-T

http://identifiers.org/hco/8/GRCh38#6758553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18933085-C-A

6758553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18933085-C-G

6758553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18933085-C-T

6758567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18933099-C-G

http://identifiers.org/hco/8/GRCh38#6758717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18933213-C-A

6759144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18933645-T-C

6759144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18933645-T-G

6759169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18933669-T-C

6759220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18933997-A-G

6759456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18934227-G-T

6759771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18934540-T-C

6759790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18934560-T-A

6760014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18934735-C-T

http://identifiers.org/hco/8/GRCh38#6760056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18934793-A-C

6760491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18934966-G-C

6760751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935141-A-G

6760769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935156-A-G

6760774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935162-G-T

6760849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935240-T-C

6761062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935831-A-G

6761091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935856-A-G

6761239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935959-T-C

6761264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935983-G-A

6761264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18935983-G-C

6761388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20886
most severe consequence: 3 prime UTR variant
orthologous variants: 18936134-C-T