163414027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 10538748-G-T

http://identifiers.org/hco/6/GRCh38#163414097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#10538679-C-A

163414097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10538679-C-T

163414168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10538588-T-C

163414170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10538586-A-G

163414214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10538506-C-T

163414242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 10538478-G-A

163414242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 10538478-G-T

http://identifiers.org/hco/6/GRCh38#163414252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10538473-C-A

163414257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 10538468-G-A

163414257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 10538468-G-C

http://identifiers.org/hco/6/GRCh38#163414324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10538425-C-A

http://identifiers.org/hco/6/GRCh38#163414363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10538403-C-A

163414363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10538403-C-T

163414632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 10538310-G-A

163414632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 10538310-G-T

163414799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10538144-G-A

http://identifiers.org/hco/6/GRCh38#163414893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10538082-C-A

163414893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10538082-C-G

163414893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10538082-C-T

163414912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10538066-T-C

163415170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 10537824-G-A

163415170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 10537824-G-T

163415314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 10537680-C-T

163415709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537449-C-T

163415947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537283-T-C

163416061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537154-G-A

163416061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537154-G-C

163416061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537154-G-T

163416087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537128-G-A

163416087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537128-G-T

163416576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10536668-G-A

163416631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10536617-T-G

163417479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535894-G-T

163418050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535392-T-G

163418107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535337-G-T

163419712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10533888-G-A

163419712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10533888-G-T

163419806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10533804-T-C

163419863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10533748-A-T

http://identifiers.org/hco/6/GRCh38#163420433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10533228-A-C

163420433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10533228-A-T

http://identifiers.org/hco/6/GRCh38#163420702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10532965-C-A

163420702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532965-C-T

163420875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532763-A-G

163420929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532709-C-T

163421332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532325-C-G

163421333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532324-C-G

163421333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532324-C-T

163422778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10531897-A-G

163422778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10531897-A-T

163423568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10531098-G-T

163423885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530736-G-A

163423926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530695-C-T

163423945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530677-C-G

163423945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530677-C-T

163424957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530069-T-C

163425041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530004-C-G

163425041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530004-C-T

163425250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10529754-A-G

163425632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10529249-T-G

163427290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10526156-G-T

163428302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10525295-T-G

163428571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10525047-G-A

163429370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10524173-T-C

163429556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10523937-A-G

163429838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10523682-C-T

163429876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10523643-C-G

163429876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10523643-C-T

163432096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10522579-G-T

163432177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10522503-T-G

163433586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10521394-G-A

http://identifiers.org/hco/6/GRCh38#163433681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10521349-C-A

163433681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10521349-C-T

163433936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10521139-T-C

163433963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10521112-T-A

163434936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10520521-T-G

163435018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10520435-A-G

http://identifiers.org/hco/6/GRCh38#163435083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10520356-A-C

163435835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10519441-C-T

163436246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10518979-G-A

http://identifiers.org/hco/6/GRCh38#163437157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10518407-C-A

163439204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10514720-A-G

163440493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10514067-T-G

http://identifiers.org/hco/6/GRCh38#163442707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10512977-A-C

163442754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10512929-T-C

163442929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10512739-C-G

http://identifiers.org/hco/6/GRCh38#163442932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10512736-A-C

163450624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10506596-A-G

163450734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10506478-A-G

163450755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10506457-T-A

163452466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10505497-C-T

163452469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10505494-G-A

163452509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10505460-T-G

163452592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10505365-G-A

163452662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10505295-T-C

163452662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10505295-T-G

163454180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10502904-C-G

163454324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10502754-G-A

163455035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10502133-G-A

163455143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10502033-A-G

http://identifiers.org/hco/6/GRCh38#163455197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10501979-C-A

163455197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10501979-C-G

http://identifiers.org/hco/6/GRCh38#163455201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10501975-C-A

163455201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10501975-C-G

163455259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10501928-A-G

163455344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 10501843-G-A

163455344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 10501843-G-C

163467528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10499114-T-C

163468858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10496963-G-T

163468932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10496897-A-G

163468932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10496897-A-T

163469270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10496606-A-G

163469850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10495598-T-C

163469904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10495572-T-C

163478684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10493080-A-T

163478902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10492868-T-A

163479835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10492036-T-C

163480175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491657-C-G

163480175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491657-C-T

163480176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491656-G-A

163480259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491591-T-C

163480259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491591-T-G

163480260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491590-T-A

http://identifiers.org/hco/6/GRCh38#163480269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10491581-C-A

163480269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491581-C-G

163480269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491581-C-T

163480362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10491526-A-G

163481332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10489371-T-C

163481333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10489370-A-G

163481336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10489367-A-G

http://identifiers.org/hco/6/GRCh38#163486078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10487576-A-C

163486078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10487576-A-G

163486196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10487452-A-G

163486318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10487308-T-C

163486385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10487223-A-G

163486430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10487192-T-G

163486972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10486548-G-A

163486990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10486501-A-T

163487334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10486092-T-C

163487369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10486056-T-C

163490266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10482581-T-C

163490860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10478862-T-C

163491167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10477171-C-T

163491298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10477048-C-G

163491396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10476969-A-G

163491428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10476935-G-A

163492292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10476249-T-C

163497501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10474821-G-T

163497696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10474589-A-T

163499893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10472829-G-A

163500260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10472412-G-A

http://identifiers.org/hco/6/GRCh38#163500518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10472187-C-A

163501562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10470401-T-G

163501667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10470296-G-A

163501711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10470248-T-C

163534554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10458356-C-T

163534778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10458203-C-G

163534809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10458176-G-T

163534849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10458138-T-A

163534889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10458094-A-G

163535333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10457001-T-A

163535464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10456921-T-C

163535487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10456915-A-T

163536317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10456236-T-C

163540502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10452186-A-G

163541384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10449181-G-C

163541791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10448886-C-G

163541909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10448775-A-G

163542561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10448181-A-G

163543613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10447109-C-T

163544618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10446441-C-T

http://identifiers.org/hco/6/GRCh38#163544706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10446363-A-C

163544706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10446363-A-G

163545051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10446026-G-T

163545903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10445167-A-G

http://identifiers.org/hco/6/GRCh38#163546240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10444927-C-A

163546275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10444893-T-C

163547312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10444077-A-G

163547731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10443728-C-T

163558062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10439185-A-G

163559291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10438499-T-C

163559351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10438459-T-C

163560499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10437457-G-C

http://identifiers.org/hco/6/GRCh38#163561923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10436787-A-C

163561923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10436787-A-G

163561923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10436787-A-T

163564084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10434742-T-G

163564168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10434670-T-C

163564168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10434670-T-G

163564408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10434635-A-G

163564596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10434472-A-G

http://identifiers.org/hco/6/GRCh38#163564903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10434142-C-A

163564903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10434142-C-G

163564903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10434142-C-T

163565000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10434051-G-A

163565028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10434023-G-T

163565289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433763-G-A

163565289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433763-G-T

163565302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433750-C-G

163565302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433750-C-T

163565427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433662-T-C

http://identifiers.org/hco/6/GRCh38#163565446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10433643-A-C

163565446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433643-A-G

163565446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433643-A-T

163565532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433560-G-A

163565532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433560-G-T

163565670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10433406-G-T

163566388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10432679-T-A

http://identifiers.org/hco/6/GRCh38#163566869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10432212-A-C

163566869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10432212-A-G

163566869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10432212-A-T

163567079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431986-G-C

163567079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431986-G-T

163567146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431919-G-T

163567196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431869-G-C

163567208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431853-A-G

163567602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431475-A-T

http://identifiers.org/hco/6/GRCh38#163567684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10431385-A-C

163567684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431385-A-G

http://identifiers.org/hco/6/GRCh38#163567696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10431373-C-A

163567704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431365-A-G

163567919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431228-G-A

163567919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431228-G-C

163567919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431228-G-T

163568081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431079-A-G

163568081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431079-A-T

163568104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10431054-G-A

http://identifiers.org/hco/6/GRCh38#163568525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10430604-C-A

163568525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430604-C-T

http://identifiers.org/hco/6/GRCh38#163568735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10430376-C-A

163568735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430376-C-G

163568735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430376-C-T

163568865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430270-T-C

163568879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430253-G-A

163568879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430253-G-T

163568921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430203-A-G

163569195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10430059-A-G

163569581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10429669-A-G

163569651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10429600-T-C

163569657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10429594-A-G

163570611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10428637-G-A

163570611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10428637-G-T

163570907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10428356-T-G

http://identifiers.org/hco/6/GRCh38#163571345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10427914-A-C

163571345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10427914-A-G

163571672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10427582-A-G

163571672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10427582-A-T

163572092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10427162-T-A

163572092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10427162-T-C

http://identifiers.org/hco/6/GRCh38#163572488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10426793-C-A

163572557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10426723-A-G

163572773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10426521-C-T

http://identifiers.org/hco/6/GRCh38#163572984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10426311-C-A

163574251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10425051-A-T

163574268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10425035-G-A

163574268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10425035-G-T

163574607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10424779-T-G

163574660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10424729-G-A

163574778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10424603-A-G

163575044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10424409-A-G

163575456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10424032-T-A

163575531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423961-G-A

163575608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423868-A-G

163575632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423829-C-T

http://identifiers.org/hco/6/GRCh38#163575645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10423816-C-A

163575655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423797-C-T

163575665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423789-A-G

163575682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423772-G-T

163575820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423717-G-T

163576014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423551-A-G

163576329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423210-T-C

163576329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423210-T-G

163576360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423175-G-A

163576360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423175-G-C

163576360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423175-G-T

163576361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423174-T-A

163576361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423174-T-C

http://identifiers.org/hco/6/GRCh38#163576369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#10423151-A-C

163576369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423151-A-G

163576521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10423006-G-A

163576601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10422894-A-G

163576859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10422653-A-G

163576985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21100
most severe consequence: 3 prime UTR variant
orthologous variants: 10422543-T-C